meddevicedb.com FDA Device Reference

COSMET

K933465 Class I Traditional
Decision Date
1994-07-20
Sponsor / Applicant
Great Bay Medical Products, Inc.

Technical Specification

510(k) Submission ID K933465
Product Code KCZ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3800
Decision Date 1994-07-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COSMET received FDA 510(k) clearance under submission number K933465, sponsored by Great Bay Medical Products, 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 1994-07-20.

Classification & Regulation

This clearance is catalogued under FDA product code KCZ and 21 CFR 878.3800, within the General, Plastic Surgery review panel as a Class I device.