meddevicedb.com FDA Device Reference

LIFE CLIP AND LIFE CLIP APPLIER

K943159 Class II Traditional
Decision Date
1994-08-16
Sponsor / Applicant
Life Surgery, Inc.

Technical Specification

510(k) Submission ID K943159
Product Code FZP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4300
Decision Date 1994-08-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIFE CLIP AND LIFE CLIP APPLIER received FDA 510(k) clearance under submission number K943159, sponsored by Life Surgery, 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 1994-08-16.

Classification & Regulation

This clearance is catalogued under FDA product code FZP and 21 CFR 878.4300, within the General, Plastic Surgery review panel as a Class II device.