American Edwards Laboratories - FDA 510(k) Cleared Devices
89
Total
88
Cleared
0
Denied
American Edwards Laboratories has 88 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 88 cleared submissions from 1980 to 1987. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by American Edwards Laboratories Filter by specialty or product code using the sidebar.
89 devices
Cleared
Dec 03, 1987
EDSLAB (R) OCCLUSION BALLOON CATHETER
Cardiovascular
94d
Cleared
Sep 30, 1987
TRANTEC DISPOSABLE PRESSURE TRANS.53-600/F/F30
Cardiovascular
90d
Cleared
Sep 15, 1987
THERMODILUTION CARDIAC OUTPUT COMPUTER, MOD. COM-2
Cardiovascular
81d
Cleared
Apr 17, 1987
HOMEPRO II VOLUMETRIC INFUSION PUMP
General Hospital
73d
Cleared
Feb 27, 1987
MEDTRAC VP VOLUMETRIC INFUSION PUMP
General Hospital
67d
Cleared
Jan 06, 1987
SHEAR FORCE GAUGE
Cardiovascular
63d
Cleared
Jan 02, 1987
VEIN VALVE CUTTER
Cardiovascular
169d
Cleared
Nov 20, 1986
CHIN-FOGARTY INFLATION DEVICE
Cardiovascular
66d
Cleared
Nov 20, 1986
MODIFICATION OF CARPENTIER-EDWARDS BIOPROSTHESIS
Cardiovascular
28d
Cleared
Oct 31, 1986
XENON LIGHT SOURCE FOR ENDOSCOPIC PROCEDURES
Orthopedic
17d
Cleared
Oct 24, 1986
FLEXIBLE VISUALIZATION CATHETER
Gastroenterology & Urology
86d
Cleared
Oct 03, 1986
DISPOSABLE BLADES FOR ARTHROSCOPIC SURGICAL DEVICE
General & Plastic Surgery
17d
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