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SUNSCENE TANNING STUDIO

K803189 Class II Traditional
Decision Date
1981-01-28
Sponsor / Applicant
Sunscene Tanning Studio

Technical Specification

510(k) Submission ID K803189
Product Code LEJ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4635
Decision Date 1981-01-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUNSCENE TANNING STUDIO received FDA 510(k) clearance under submission number K803189, sponsored by Sunscene Tanning Studio. 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 1981-01-28.

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.