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ELECTROSURGICAL UNIT 774

K850668 Class II Traditional
Decision Date
1985-05-20
Sponsor / Applicant
Birtcher Corp.

Technical Specification

510(k) Submission ID K850668
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1985-05-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTROSURGICAL UNIT 774 received FDA 510(k) clearance under submission number K850668, sponsored by Birtcher Corp.. 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 1985-05-20.

Classification & Regulation

This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.