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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Light, Ultraviolet, Dermatological
510(k) Number K840137
Device Name SILGMANN SOLARIUM S-TYPE 1218 COMBO
Applicant
TANNHUT
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
TANNHUT
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number878.4630
Classification Product Code
FTC  
Date Received01/10/1984
Decision Date 04/23/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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