meddevicedb.com FDA Device Reference

DISP. MICROSURGICAL KNIVES

K821737 Class I Traditional
Decision Date
1982-07-02
Sponsor / Applicant
Coburn Optical Ind., Inc.

Technical Specification

510(k) Submission ID K821737
Product Code GES
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1982-07-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISP. MICROSURGICAL KNIVES received FDA 510(k) clearance under submission number K821737, sponsored by Coburn Optical Ind., 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 1982-07-02.

Classification & Regulation

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