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SILGMANN SOLARIUM S-TYPE 1218 COMBO

K840137 Class II Traditional
Decision Date
1984-04-23
Sponsor / Applicant
Tannhut

Technical Specification

510(k) Submission ID K840137
Product Code FTC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4630
Decision Date 1984-04-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SILGMANN SOLARIUM S-TYPE 1218 COMBO received FDA 510(k) clearance under submission number K840137, sponsored by Tannhut. 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 1984-04-23.

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.