American Bentley - FDA 510(k) Cleared Devices
59
Total
59
Cleared
0
Denied
American Bentley has 59 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 59 cleared submissions from 1983 to 1988.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
59 devices
Cleared
Feb 12, 1988
UMBILICAL ARTERY OXYGEN PROBE MODEL UAP-100
Anesthesiology
204d
Cleared
Nov 06, 1987
INTEGRATED MEMBRANE OXYGENATOR W/CARDIOTOMY FILTER
Cardiovascular
42d
Cleared
Sep 01, 1987
CARDIOPLEGIA HEAT EXCHANGER MODEL NO. HE-100
Cardiovascular
186d
Cleared
Sep 01, 1987
CARDIOTOMY/MEDIASTINAL AUTO. RESERVOIR CATR-3500
Cardiovascular
85d
Cleared
Aug 24, 1987
OXYGENATOR MODEL NO. BENTLEY 5 PLUS
Cardiovascular
83d
Cleared
May 29, 1987
INDWELLING BLOOD CARBONDIOXIDE PARTIAL PRES. ANALY
Anesthesiology
84d
Cleared
Mar 09, 1987
ELECTROSURGICAL MENISCUS CUTTER (EMC) MOD. AMC-100
General & Plastic Surgery
45d
Cleared
Oct 20, 1986
OXYGENATOR MODEL NO. BENTLEY-10 PLUS
Cardiovascular
59d
Cleared
Sep 29, 1986
HEPARIN-COATED EXTRACORPOREAL CIRCUITS
Cardiovascular
152d
Cleared
Jul 15, 1986
ARTERIAL BLOOD FILTER HOLDER MODEL NO. AF-HE
Cardiovascular
12d
Cleared
Jun 26, 1986
OXYGENATOR MODEL NOS. BENTLEY-10A & BENTLEY-10B
Cardiovascular
122d
Cleared
Mar 03, 1986
ADJUSTABLE OXYGENATOR HOLDER MODEL NO. BCM-HL
Cardiovascular
7d
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