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BIPOLAR FORCEPS

K792365 Class II Traditional
Decision Date
1979-12-10
Sponsor / Applicant
Concept, Inc.

Technical Specification

510(k) Submission ID K792365
Product Code JOS
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1979-12-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIPOLAR FORCEPS received FDA 510(k) clearance under submission number K792365, sponsored by Concept, 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 1979-12-10.

Classification & Regulation

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