meddevicedb.com FDA Device Reference

ULTRA-VIOLET A SOURCE LIGHT EMITTING

K842575 Class II Traditional
Decision Date
1984-08-10
Sponsor / Applicant
Sola-Tan Intl.

Technical Specification

510(k) Submission ID K842575
Product Code FTC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4630
Decision Date 1984-08-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ULTRA-VIOLET A SOURCE LIGHT EMITTING received FDA 510(k) clearance under submission number K842575, sponsored by Sola-Tan Intl.. 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 1984-08-10.

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.