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

BLOOD CARDIOPLEGIA HEAT EXCHANGER, MODEL #HE-30

K Number: K913956 · Decision Jan 17, 1992
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
168
Applicant Total
55
Review Days
134

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Basic Information

Device Name
BLOOD CARDIOPLEGIA HEAT EXCHANGER, MODEL #HE-30
K Number
K913956
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4400
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bentley Laboratories, Inc.
Date Received
September 5, 1991
Decision Date
January 17, 1992
Product Code
DTN
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
DTN Reservoir, Blood, Cardiopulmonary Bypass

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Other Clearances by Bentley Laboratories, Inc.

K Number Device Name
K931967 HE-30 GOLD
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K903641 QUICK PRIME HEMOCONCEN. NO. HQ-7000 AND CBP-7000Q
K894826 UNIVOX W/HOLDERS, MODELS UNIVOX-HL, HLB, HLF
K874841 INTEGRATED MEMBRANE OXYGENATOR W/CARDIOTOMY FILTER
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. →