Medical Devices; Gastroenterology-Urology Devices; Classification of the Endoscopic Electrosurgical Clip Cutting System. Final order [0.03%]
医疗器械；胃肠病和泌尿科器械；终官方决定：内窥镜电外科夹切系统分类
Food and Drug Administration, HHS
Food and Drug Administration
The Food and Drug Administration (FDA or we) is classifying the endoscopic electrosurgical clip cutting system into class II (special controls). The special controls that apply to the device type are identified in this order and will be par...
Medical Devices; Immunology and Microbiology Devices; Classification of the Brain Trauma Assessment Test. Final order [0.03%]
医疗器械；免疫和微生物学器械；脑损伤评估试验的分类。最终命令
Food and Drug Administration, HHS
Food and Drug Administration
The Food and Drug Administration (FDA or we) is classifying the brain trauma assessment test into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified ...
Office of Workers’ Compensation Programs, Labor.
Office of Workers’ Compensation Programs
This final rule revises the regulations under the Black Lung Benefits Act (BLBA or Act) governing the payment of medical benefits and maintains the level of care available to miners. The final rule establishes methods for determining the am...
Process for Department of Veterans Affairs (VA) Physicians To Be Added to the National Registry of Certified Medical Examiners. Final rule [0.03%]
关于美国退伍军人事务部(VA)医生加入全国认证机动车检验员注册系统的程序的规定（最终规则）
Federal Motor Carrier Safety Administration, (FMCSA), DOT
Federal Motor Carrier Safety Administration
FMCSA amends the Federal Motor Carrier Safety Regulations (FMCSRs) to establish an alternative process for qualified advanced practice nurses, doctors of chiropractic, doctors of medicine, doctors of osteopathy, physician assistants, and ot...
Medicare Program; Changes to the Comprehensive Care for Joint Replacement Payment Model (CJR): Extreme and Uncontrollable Circumstances Policy for the CJR Model. Final rule [0.03%]
医疗保险程序；对综合关节置换术支付模式（CJR）的变化：极端和不可控情况的CJR模式政策。最终规则
Centers for Medicare & Medicaid Services (CMS), HHS
Centers for Medicare & Medicaid Services (CMS)
This final rule finalizes a policy that provides flexibility in the determination of episode spending for Comprehensive Care for Joint Replacement Payment Model (CJR) participant hospitals located in areas impacted by extreme and uncontroll...
Medical Devices; Orthopedic Devices; Classification of the In Vivo Cured Intramedullary Fixation Rod. Final order [0.03%]
医疗器械；骨科器械； intramedullary fixation rod（髓内固定杆）的定类决定（最终令）
Food and Drug Administration, HHS
Food and Drug Administration
The Food and Drug Administration (FDA or we) is classifying the in vivo cured intramedullary fixation rod into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of ...
Medical Devices; General and Plastic Surgery Devices; Classification of the Microneedling Device for Aesthetic Use. Final order [0.03%]
医疗器械；一般和整形外科器械；用于美容的微针器械分类。最终命令
Food and Drug Administration, HHS
Food and Drug Administration
The Food and Drug Administration (FDA or we) is classifying the microneedling device for aesthetic use into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the...
Medicare Program; Update to the Required Prior Authorization List of Durable Medical Equipment, Prosthetics, Orthotics, and Supplies (DMEPOS) Items That Require Prior Authorization as a Condition of Payment. Update to list [0.03%]
关于医保 durable medical equipment、prosthetics、orthotics 和 supplies (dmepos) 需要预先授权清单的更新通知
Centers for Medicare & Medicare Services (CMS), HHS
Centers for Medicare & Medicare Services (CMS)
This document announces the addition of 31 Healthcare Common Procedure Coding System (HCPCS) codes to the Required Prior Authorization List of Durable Medical Equipment, Prosthetics, Orthotics, and Supplies (DMEPOS) Items that require prior...
Medical Devices; Exemptions From Premarket Notification: Class II Devices. Final order [0.03%]
医疗器械；免于提交510（k）上市前通知的器械分类决定的最终命令
Food and Drug Administration, HHS
Food and Drug Administration
The Food and Drug Administration (FDA or the Agency) is publishing an order to exempt a list of class II devices from premarket notification (510(k)) requirements, subject to certain limitations. This exemption from 510(k), subject to certa...
Hearing Aid Compatibility Standards. Final rule; announcement of effective date [0.03%]
助听设备兼容性标准终版规则；生效日期公告
Federal Communications Commission
Federal Communications Commission
In this document, the Commission announces that the Office of Management and Budget (OMB) has approved, for a period of three years, the information collection associated with rules adopted in the Commission’s document Access to Telecommun...