FDA 510(k) Applications Submitted by MARIANNE D DRENNAN
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| 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. |
| 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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