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Megadyne Smoke Evacuator, Megadyne Filter, Megadyne Fluid Trap, Megadyne Connect Cable, 1 m and 2.1 m, Megadyne RF Sensor

K200250 Class II Traditional
Decision Date
2020-06-26
Sponsor / Applicant
Megadyne Medical Products, Inc.

Technical Specification

510(k) Submission ID K200250
Product Code FYD
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5070
Decision Date 2020-06-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Megadyne Smoke Evacuator, Megadyne Filter, Megadyne Fluid Trap, Megadyne Connect Cable, 1 m and 2.1 m, Megadyne RF Sensor received FDA 510(k) clearance under submission number K200250, sponsored by Megadyne Medical Products, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2020-06-26.

Classification & Regulation

This clearance is catalogued under FDA product code FYD and 21 CFR 878.5070, within the General, Plastic Surgery review panel as a Class II device.