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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Apparatus, Suction, Single Patient Use, Portable, Nonpowered
510(k) Number K901742
Device Name INAMED SMALL DRAIN SYSTEM
Applicant
Inamed Development Co.
1035 A. Cindy Ln.
Carpinteria,  CA  93013
Applicant Contact ELLEN DUKE
Correspondent
Inamed Development Co.
1035 A. Cindy Ln.
Carpinteria,  CA  93013
Correspondent Contact ELLEN DUKE
Regulation Number878.4680
Classification Product Code
GCY  
Date Received04/17/1990
Decision Date 05/07/1990
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
Predetermined Change
Control Plan Authorized		 No
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