meddevicedb.com FDA Device Reference

Universal Light Handle Cover, Light Handle Cover

K150532 Class II Traditional
Decision Date
2015-09-22
Sponsor / Applicant
Key Surgical, Inc.

Technical Specification

510(k) Submission ID K150532
Product Code FTA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4580
Decision Date 2015-09-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Universal Light Handle Cover, Light Handle Cover received FDA 510(k) clearance under submission number K150532, sponsored by Key Surgical, 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 2015-09-22.

Classification & Regulation

This clearance is catalogued under FDA product code FTA and 21 CFR 878.4580, within the General, Plastic Surgery review panel as a Class II device.