meddevicedb.com FDA Device Reference

FORCE GSU SYSTEM MODEL NO. GSU-20 AND GSU-22

K942579 Class II Traditional
Decision Date
1994-09-21
Sponsor / Applicant
Valleylab, Inc.

Technical Specification

510(k) Submission ID K942579
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1994-09-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FORCE GSU SYSTEM MODEL NO. GSU-20 AND GSU-22 received FDA 510(k) clearance under submission number K942579, sponsored by Valleylab, 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 1994-09-21.

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.