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

EXPANDED USE OF HARDSHELL VENOUS RESERV. W/FILTER

K Number: K872719 · Decision Sep 30, 1987
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
168
Applicant Total
174
Review Days
82

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Basic Information

Device Name
EXPANDED USE OF HARDSHELL VENOUS RESERV. W/FILTER
K Number
K872719
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4400
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Shiley, Inc.
Date Received
July 10, 1987
Decision Date
September 30, 1987
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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