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HOT BIOPSY FORCEPS W/ROUND CUPS

K820983 Class II Traditional
Decision Date
1982-04-26
Sponsor / Applicant
Mill-Rose Laboratory

Technical Specification

510(k) Submission ID K820983
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1982-04-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOT BIOPSY FORCEPS W/ROUND CUPS received FDA 510(k) clearance under submission number K820983, sponsored by Mill-Rose Laboratory. 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 1982-04-26.

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.