meddevicedb.com FDA Device Reference

TISSUE FORCEPS

K822591 Class I Traditional
Decision Date
1982-10-13
Sponsor / Applicant
Medcare Products

Technical Specification

510(k) Submission ID K822591
Product Code GEN
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1982-10-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TISSUE FORCEPS received FDA 510(k) clearance under submission number K822591, sponsored by Medcare Products. 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 1982-10-13.

Classification & Regulation

This clearance is catalogued under FDA product code GEN and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.