meddevicedb.com FDA Device Reference

ALPHA SOLAR SYSTEM TANNING BED

K943656 Class II Traditional
Decision Date
1994-08-15
Sponsor / Applicant
Heartland Tan Systems

Technical Specification

510(k) Submission ID K943656
Product Code LEJ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4635
Decision Date 1994-08-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALPHA SOLAR SYSTEM TANNING BED received FDA 510(k) clearance under submission number K943656, sponsored by Heartland Tan Systems. 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 1994-08-15.

Classification & Regulation

This clearance is catalogued under FDA product code LEJ and 21 CFR 878.4635, within the General, Plastic Surgery review panel as a Class II device.