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

MODIFIED PYROGEN TESTING

K Number: K910935 · Decision May 16, 1991
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
95
Applicant Total
41
Review Days
91

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Basic Information

Device Name
MODIFIED PYROGEN TESTING
K Number
K910935
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4260
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Electromedics, Inc.
Date Received
February 14, 1991
Decision Date
May 16, 1991
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

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K934355 ELECTROMEDICS BLOOD HEAT EXCHANGER
K930154 EL2-SERIES BLOOD COLLECTION REERVOIR
K926250 ELECTROMEDICS EL-SERIES CARDIOTOMY RESERVOIR
K925412 ELECTROMEDICS TISSUE TRAP/ #TT280
K915737 AUTOTRANSFUSION BLOOD COLLECTION RESERVOIR
K910238 PORTABLE AUTO TRANSFUSION SYSTEM 500
K902723 ARTERIAL BLOOD FILTER ELECTRO. AIR* STAR 40 AND 20
K903392 ELECTROMEDICS BT422-120 AND BT422-40
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