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

HAND-HELD INTRACARDIAC SUCKERS W/ERGONOMIC HANDLES

K Number: K900339 · Decision Mar 28, 1990
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
8
Applicant Total
174
Review Days
64

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Basic Information

Device Name
HAND-HELD INTRACARDIAC SUCKERS W/ERGONOMIC HANDLES
K Number
K900339
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4420
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Shiley, Inc.
Date Received
January 23, 1990
Decision Date
March 28, 1990
Product Code
DTS
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
DTS Sucker, Cardiotomy Return, 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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