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

FILTER, INFUSION BLOOD (1 PFF-100)

K Number: K760165 · Decision Aug 6, 1976
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
35
Applicant Total
55
Review Days
31

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Basic Information

Device Name
FILTER, INFUSION BLOOD (1 PFF-100)
K Number
K760165
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Bentley Laboratories, Inc.
Date Received
July 6, 1976
Decision Date
August 6, 1976
Product Code
CAK
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
CAK Microfilter, Blood Transfusion

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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
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