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NORDIC SUN HOME TANNING UNIT

K860567 Class II Traditional
Decision Date
1986-03-05
Sponsor / Applicant
Nordic Sun Corporation of America

Technical Specification

510(k) Submission ID K860567
Product Code FTC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4630
Decision Date 1986-03-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NORDIC SUN HOME TANNING UNIT received FDA 510(k) clearance under submission number K860567, sponsored by Nordic Sun Corporation of America. 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 1986-03-05.

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.