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

PEDIATRIC ARTERIAL BLOOD FILTER #AF-5

K Number: K801147 · Decision Jun 4, 1980
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
95
Applicant Total
55
Review Days
22

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
PEDIATRIC ARTERIAL BLOOD FILTER #AF-5
K Number
K801147
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4260
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Bentley Laboratories, Inc.
Date Received
May 13, 1980
Decision Date
June 4, 1980
Product Code
DTM
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
DTM Filter, Blood, Cardiopulmonary Bypass, Arterial Line

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DTM), ordered by most recent decision date.

View all

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
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
Search all 55 clearances from Bentley Laboratories, Inc. →