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) number: K233644
Device name: 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)
Applicant: Megadyne Medical Products, Inc. OH · US
Product code: GEI — Electrosurgical, Cutting & Coagulation & Accessories
Decision date: 2024-07-12
Date received: 2023-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Advisory committee: General, Plastic Surgery

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

Official FDA record: K233644

Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.