Medtronic Bio-Medicus, Inc. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Medtronic Bio-Medicus, Inc. has 13 FDA 510(k) cleared cardiovascular devices. Based in Eden Prairie, US.
Historical record: 13 cleared submissions from 1992 to 1998.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
13 devices
Cleared
Apr 27, 1998
CSS-CARDIOPLEGIA SAFETY SYSTEM
Cardiovascular
242d
Cleared
Feb 25, 1998
BPX80 BIO-PUMP (BPX80)
Cardiovascular
196d
Cleared
Jan 16, 1996
BIOTREND OXYGEN SATURATION & HEMATOCRIT SYSTEM
Cardiovascular
110d
Cleared
Feb 17, 1995
MEDSAT OXYGEN SATURATION SYSTEM
Cardiovascular
303d
Cleared
Dec 23, 1994
MEDTRONIC BIO-MEDICUS BIO-CONSOLE MODEL 550M PUMP SPEED CONTROLLER
Cardiovascular
366d
Cleared
Jul 20, 1994
BIO-MEDICUS BIO-CONSOLE MODELS 540, 540A,B,C,D,E, & 550
Cardiovascular
91d
Cleared
Jul 08, 1993
BIO-PROBE(R) BLOOD FLOW MONITORING SYST(TX-50/50P)
Cardiovascular
322d
Cleared
Jun 02, 1993
MEDTRONIC BIO-MEDICUS HANDCRANK MODEL 150
Cardiovascular
163d
Cleared
May 07, 1993
MEDTRONIC BIO-MEDICUS BIO-CONSOLE MODEL 540E
Cardiovascular
260d
Cleared
May 06, 1993
MEDTRONIC BIO-MEDICUS BIO-CONSOLE MODEL 550
Cardiovascular
259d
Cleared
Mar 26, 1993
MEDTRONIC BIO-MEDICUS FEMORAL CANNULA/INTRODUCER
Cardiovascular
193d
Cleared
Dec 08, 1992
MEDTRONIC BIO-MEDICUS CANNULA INSERTION KIT
Cardiovascular
85d
Cleared
May 20, 1992
MEDTRONIC BIO-MEDICUS BIO-CONSOLE MODEL 540-D
Cardiovascular
211d