meddevicedb.com FDA Device Reference

THE SUNTANNING CO. TANNING BED

K852579 Class II Traditional
Decision Date
1985-07-03
Sponsor / Applicant
The Suntanning Company, Inc.

Technical Specification

510(k) Submission ID K852579
Product Code FTC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4630
Decision Date 1985-07-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THE SUNTANNING CO. TANNING BED received FDA 510(k) clearance under submission number K852579, sponsored by The Suntanning Company, 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 1985-07-03.

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.