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

DIDECO-SHILEY AUTOTRANSFUSION CARDIOTOMY RESERVOIR

K Number: K893711 · Decision Feb 28, 1990
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
168
Applicant Total
174
Review Days
286

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Basic Information

Device Name
DIDECO-SHILEY AUTOTRANSFUSION CARDIOTOMY RESERVOIR
K Number
K893711
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4400
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Shiley, Inc.
Date Received
May 18, 1989
Decision Date
February 28, 1990
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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K910923 BCD ADVANCED
K901548 BIOMEDICAL SENSORS-SHILEY BGM 4000 INTRA BLOOD GAS
K903435 SHILEY SPECIALIZED TRACHEOSTOMY TUBE
K901624 SHILEY PLEXUS INTEGRAL RESERVOIR HOLLOW FIBER OXY.
K901250 PLEXUS 2(TM) INFANT HOLLOW FIBER OXYGENATOR
K901249 PLEXUS 3.5(TM) PEDIATRIC HOLLOW FIBER OXYGENATOR
K900797 STOCKERT SHILEY DUAL PRESSURE CONTROL MODULE XR
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