meddevicedb.com FDA Device Reference

PHOTOTHERAPY LIGHT

K760872 Class II Traditional
Decision Date
1976-11-02
Sponsor / Applicant
Air-Shields, Inc.

Technical Specification

510(k) Submission ID K760872
Product Code LBI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5700
Decision Date 1976-11-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHOTOTHERAPY LIGHT received FDA 510(k) clearance under submission number K760872, sponsored by Air-Shields, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1976-11-02.

Classification & Regulation

This clearance is catalogued under FDA product code LBI and 21 CFR 880.5700, within the General Hospital review panel as a Class II device.