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SUN ROOM TANNING BOOTH

K801674 Class II Traditional
Decision Date
1980-09-16
Sponsor / Applicant
Sun Tan Enterprises, Inc.

Technical Specification

510(k) Submission ID K801674
Product Code LEJ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4635
Decision Date 1980-09-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUN ROOM TANNING BOOTH received FDA 510(k) clearance under submission number K801674, sponsored by Sun Tan Enterprises, 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 1980-09-16.

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.