Burron Medical, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Burron Medical, Inc. has 9 FDA 510(k) cleared medical devices. Based in Bethlehem, US.
Historical record: 9 cleared submissions from 1988 to 1991. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Burron Medical, Inc. Filter by specialty or product code using the sidebar.
9 devices
Cleared
Oct 08, 1991
CELSITE(TM) IMPLANTABLE DRUG DELIVERY SYSTEM
General Hospital
496d
Cleared
May 09, 1990
BURRON AMBULATORY DRUG DELIVERY SYSTEM
General Hospital
182d
Cleared
Mar 06, 1990
COMBITRANS DISPOSABLE PRESSURE TRANSDUCER KIT
Cardiovascular
515d
Cleared
Nov 24, 1989
ANTI-THROMBOGENIC COATING FOR CATHETERS
General Hospital
105d
Cleared
Sep 18, 1989
SPINOCAN(R) CONTINUOUS SPINAL TRAY
Anesthesiology
38d
Cleared
Aug 03, 1989
BURRON TEFLON-COATED GUIDEWIRE
Cardiovascular
303d
Cleared
Aug 11, 1988
PERFUSOR M SYRINGE PUMP
General Hospital
85d
Cleared
Aug 11, 1988
PERFUSOR SECURA SYRINGE PUMP
General Hospital
84d
Cleared
Aug 09, 1988
IMPLANTOFIX II IMPLANTABLE DRUG DELIVERY SYSTEM
General Hospital
132d