Bentley Laboratories, Inc. - FDA 510(k) Cleared Devices
55
Total
55
Cleared
0
Denied
FDA 510(k) Regulatory Record - Bentley Laboratories, Inc. Cardiovascular ✕
44 devices
Cleared
Jul 13, 1993
HE-30 GOLD
Cardiovascular
83d
Cleared
Jan 17, 1992
BLOOD CARDIOPLEGIA HEAT EXCHANGER, MODEL #HE-30
Cardiovascular
134d
Cleared
Nov 15, 1991
VENOUS RESERVOIR BAG MODEL NO. BMR-250(TM)
Cardiovascular
88d
Cleared
Feb 28, 1990
UNIVOX W/HOLDERS, MODELS UNIVOX-HL, HLB, HLF
Cardiovascular
212d
Cleared
Feb 02, 1988
INTEGRATED MEMBRANE OXYGENATOR W/CARDIOTOMY FILTER
Cardiovascular
70d
Cleared
Jan 19, 1988
BAXTER ACCUPORT(TM) CENTRAL VENOUS CATHETER
Cardiovascular
71d
Cleared
Jan 05, 1983
BOS-2S, SPIRAFLO BUBBLE INFANT OXYGEN.
Cardiovascular
64d
Cleared
Jan 05, 1983
OXYGEN CONSUMPTION MONITOR #OCM-0100
Cardiovascular
61d
Cleared
Dec 30, 1982
VENOUS RESERVOIR BAG #BMR-1400
Cardiovascular
58d
Cleared
Dec 30, 1982
OXYGENATORS #BOS-10, 105, 5S
Cardiovascular
42d
Cleared
Nov 01, 1982
BLOOD OXYGENATORS #BOS-105S BOS-5S W/
Cardiovascular
45d
Cleared
Jul 02, 1982
DISPOSABLE BLOOD PRESSURE TRANSDUCER
Cardiovascular
51d
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