FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

INTEGRATED MEMBRANE OXYGENATOR W/CARDIOTOMY FILTER

K Number: K874841 · Decision Feb 2, 1988
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
253
Applicant Total
55
Review Days
70

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Basic Information

Device Name
INTEGRATED MEMBRANE OXYGENATOR W/CARDIOTOMY FILTER
K Number
K874841
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4350
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Bentley Laboratories, Inc.
Date Received
November 24, 1987
Decision Date
February 2, 1988
Product Code
DTZ
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DTZ Oxygenator, Cardiopulmonary Bypass

Similar 510(k) Clearances

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Other Clearances by Bentley Laboratories, Inc.

K Number Device Name
K931967 HE-30 GOLD
K913956 BLOOD CARDIOPLEGIA HEAT EXCHANGER, MODEL #HE-30
K913692 VENOUS RESERVOIR BAG MODEL NO. BMR-250(TM)
K903641 QUICK PRIME HEMOCONCEN. NO. HQ-7000 AND CBP-7000Q
K894826 UNIVOX W/HOLDERS, MODELS UNIVOX-HL, HLB, HLF
K874867 CATR(TM)-H CARDIOTOMY HOLDER
K874618 BAXTER ACCUPORT(TM) CENTRAL VENOUS CATHETER
K823273 BOS-2S, SPIRAFLO BUBBLE INFANT OXYGEN.
K823359 OXYGEN CONSUMPTION MONITOR #OCM-0100
K823456 OXYGENATORS #BOS-10, 105, 5S
Search all 55 clearances from Bentley Laboratories, Inc. →