Megadyne Medical Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Megadyne Medical Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: 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), ETHICON Megadyne Electrosurgical Generator, Megadyne Smoke Evacuator, Megadyne Filter, Megadyne Fluid Trap, Megadyne Connect Cable, 1 m and 2.1 m, Megadyne RF Sensor
Megadyne Medical Products, Inc. has 48 FDA 510(k) cleared general & plastic surgery devices. Based in Murray, US.
Latest FDA clearance: Jul 2024. Active since 1990.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Ethicon Endo-Surgery, Inc. and Ethicon Endo-Surgery, LLC.
FDA 510(k) Regulatory Record - Megadyne Medical Products, Inc.
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