K233644

Megadyne Patient Return Electrode Pad - Universal Dual (model 0846), Megadyne Patient Return Electrode Pad - Universal Plus (model 0847), Megadyne Patient Return Electrode Pad - Universal Dual Plus (model 0848)

510(k) 号: K233644
器械名称: Megadyne Patient Return Electrode Pad - Universal Dual (model 0846), Megadyne Patient Return Electrode Pad - Universal Plus (model 0847), Megadyne Patient Return Electrode Pad - Universal Dual Plus (model 0848)
申请人: Megadyne Medical Products, Inc. OH · US
产品代码: GEI — Electrosurgical, Cutting & Coagulation & Accessories
批准日期: 2024-07-12
受理日期: 2023-11-13
决定: Substantially Equivalent
审查途径: Traditional
咨询委员会: General, Plastic Surgery

510(k) Summary（FDA 官方 PDF）： K233644.pdf

FDA 官方记录： K233644

数据来自 openFDA 510(k) 数据集（CC0 公有领域），以 FDA 现行记录为准。510(k) 许可不等于 FDA 认证或批准。