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

CARDIOTOMY/MEDIASTINAL AUTO. RESERVOIR CATR-3500

K Number: K872167 · Decision Sep 1, 1987
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
33
Applicant Total
59
Review Days
85

Basic Information

Device Name
CARDIOTOMY/MEDIASTINAL AUTO. RESERVOIR CATR-3500
K Number
K872167
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4230
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
AMERICAN BENTLEY
Date Received
June 8, 1987
Decision Date
September 1, 1987
Product Code
DTP
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
DTP Defoamer, Cardiopulmonary Bypass

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K870911 INDWELLING BLOOD CARBONDIOXIDE PARTIAL PRES. ANALY
K870269 ELECTROSURGICAL MENISCUS CUTTER (EMC) MOD. AMC-100
K863249 OXYGENATOR MODEL NO. BENTLEY-10 PLUS
K861641 HEPARIN-COATED EXTRACORPOREAL CIRCUITS
K862549 ARTERIAL BLOOD FILTER HOLDER MODEL NO. AF-HE
K860673 OXYGENATOR MODEL NOS. BENTLEY-10A & BENTLEY-10B
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