meddevicedb.com FDA Device Reference

TL100W/01 UVB LAMP

K910767 Class II Traditional
Decision Date
1991-05-23
Sponsor / Applicant
Philips Lighting Co.

Technical Specification

510(k) Submission ID K910767
Product Code FTC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4630
Decision Date 1991-05-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TL100W/01 UVB LAMP received FDA 510(k) clearance under submission number K910767, sponsored by Philips Lighting Co.. 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 1991-05-23.

Classification & Regulation

This clearance is catalogued under FDA product code FTC and 21 CFR 878.4630, within the General, Plastic Surgery review panel as a Class II device.