FDA 510(k) Applications Submitted by MARIANNE DRENNAN

FDA 510(k) Number Submission Date Device Name Applicant
K942967 06/20/1994 AUTO SUTURE SPINAL CURETTE UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
K942968 06/20/1994 AUTO SUTURE SPINAL OSTEOTOME UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
K942969 06/20/1994 AUTO SUTURE SPINAL NERVE HOOK UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
K942970 06/20/1994 AUTO SUTURE SPINAL ELEVATOR UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
K942971 06/20/1994 AUTO SUTURE SPINAL DISSECTOR UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
K943115 06/27/1994 AUTO SUTURE PITUITARY SPINAL RONGEUR UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
K943116 06/27/1994 AUTO SUTURE KERRISON SPINAL RONGEUR UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
K946029 12/09/1994 ACS GUIDE WIRES WITH MODIFIED PACKAGE INSERT ADVANCED CARDIOVASCULAR SYSTEMS, INC.
K970496 02/10/1997 HEARTPORT MAZE SYSTEM: CRYOPROBE SET HEARTPORT, INC.
K990772 03/09/1999 DIRECTFLOW ARTERIAL CANNULA HEARTPORT, INC.
K971291 04/07/1997 HEARTPORT ENDOARTERIAL RETURN CANNULA HEARTPORT, INC.
K981995 06/08/1998 QUICKDRAW VENOUS CANNULA HEARTPORT, INC.
K972570 07/10/1997 HEARTPORT INTRODUCER SHEATH HEARTPORT, INC.
K953987 08/23/1995 ACS TOURGIDE GUIDING CATHETER ADVANCED CARDIOVASCULAR SYSTEMS, INC.
K964302 10/29/1996 HEARTPORT THORACIC TROCAR HEARTPORT, INC.
K974175 11/06/1997 HEARTPORT ENDOAORTIC CLAMP CATHETER HEARTPORT, INC.
K994243 12/16/1999 DIRECTFLOW KIT, 24 FR, SOFTCLAMP KIT, 24FR, STRAIGHTSHOT KIT, 23 FR, STRAIGHT TIP, STRAIGHTSHOT KIT, 23 FR, ANGLED TIP HEARTPORT, INC.
K965051 12/18/1996 HEARTPORT NEEDLE TROCAR HEARTPORT, INC.
K974736 12/19/1997 HEARTPORT DIRECT AORTIC RETURN CANNULA WITH INTRODUCER HEARTPORT, INC.
K981009 03/18/1998 HEARTPORT ENDOPULMONARY VENT CATHETER HEARTPORT, INC.


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