Medtronic Blood Systems, Inc. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Medtronic Blood Systems, Inc. has 15 FDA 510(k) cleared cardiovascular devices. Based in Anaheim, US.
Historical record: 15 cleared submissions from 1988 to 1995.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
15 devices
Cleared
Jul 14, 1995
TEMPORARY MYOCARDIAL PACING LEAD, MODEL 6500
Cardiovascular
280d
Cleared
Jul 14, 1995
UNIPOLAR ATRIAL TEMPORARY PACING LEAD,MODEL 6492
Cardiovascular
276d
Cleared
Dec 12, 1989
CLOSED CHEST SUPPORT CIRCUIT
Cardiovascular
230d
Cleared
Nov 27, 1989
DURAN FLEXIBLE ANNULOPLASTY RING & OBTURATOR H601H
Cardiovascular
195d
Cleared
May 31, 1989
EXTRACORPOREAL CIRCUIT WITH BIO-ACTIVE SURFACE
Cardiovascular
70d
Cleared
May 19, 1989
MAXIMA* HOLLOW FIBER OXYGENATOR W/FILTERED RESERV.
Cardiovascular
73d
Cleared
Feb 22, 1989
INTERSEPT* CRYSTALLOID CARDIOPLEGIA DELIV. SYSTEM
Cardiovascular
69d
Cleared
Dec 21, 1988
INTERSEPT* CRYSTALLOID CARDIOPLEGIA FILTER
Cardiovascular
64d
Cleared
Dec 05, 1988
INTERSEPT* PREBYPASS FILTER
Cardiovascular
55d
Cleared
Oct 13, 1988
INTERSEPT*CRYSTALLOID CARDIOPLEGIA DELIVERY SYSTEM
Cardiovascular
59d
Cleared
Sep 16, 1988
INTERSEPT*PREBYPASS FILTER
Cardiovascular
57d
Cleared
Aug 12, 1988
EXTENDED SHELF LIFE FOR INTERSEPT* ARTERIAL 20/40
Cardiovascular
84d
Cleared
Aug 11, 1988
INTERSEPT* OXYGEN GAS LINE FILTER
Cardiovascular
83d
Cleared
Jul 18, 1988
26MM DIAMETER HANCOCK* TROCAR BLADE AND TIP
Cardiovascular
32d
Cleared
May 06, 1988
MODIFIED INTERSEPT PEDIATRIC BLOOD FILTER
Cardiovascular
78d