FDA 510(k) Applications for Medical Device Product Code "DWQ"
(Stripper, Vein, External)

FDA 510(k) Number Applicant Device Name Decision Date
K885046 AESCULAP INSTRUMENTS CORP. INSITUCAT VALVE STRIPPER 02/28/1990
K811910 ATRIUM MEDICAL CORP. VEIN-TRAP TM 07/20/1981
K904507 PILLING CO. PILLING BRUSH VALVULOTOME 03/01/1991
K041453 SMITH & NEPHEW, INC. SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023 07/22/2004
K032387 SMITH & NEPHEW, INC. TRIVEX SYSTEM 10/29/2003
K872157 SOLCO BASLE, INC. HALL VEIN STRIPPER 07/07/1987
K905528 URESIL CORP. URESIL VALVE CUTTER 04/18/1991


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