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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 K845001
Device Name MARTANIQUE 6-TUBE HOME SOLARIUM
Applicant
BAINBRIDGE TRADING CO., LTD.
210 SOUND BEACH AVE.
OLD GREENWICH,  CT  06870
Applicant Contact QNDREW R HUSTON
Correspondent
BAINBRIDGE TRADING CO., LTD.
210 SOUND BEACH AVE.
OLD GREENWICH,  CT  06870
Correspondent Contact QNDREW R HUSTON
Regulation Number878.4630
Classification Product Code
FTC  
Date Received12/26/1984
Decision Date 02/21/1985
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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