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

SWANK BLOOD TRANSFUSION MICRO-FILTER W/STRAIGHT SE

K Number: K855064 · Decision Mar 12, 1986
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
35
Applicant Total
77
Review Days
84

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Basic Information

Device Name
SWANK BLOOD TRANSFUSION MICRO-FILTER W/STRAIGHT SE
K Number
K855064
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Cobe Laboratories, Inc.
Date Received
December 18, 1985
Decision Date
March 12, 1986
Product Code
CAK
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CAK Microfilter, Blood Transfusion

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K905793 COBE CENTRY 2 BICART OPTION KIT
K905388 COBE CENTRYSYSTEM 3 BICART OPTION KIT
K904336 NEW COBE SATURATION/HEMATOCRIT MONITOR
K902631 COBE ICU CONVERSION KIT
K902437 COBE CARDIOTOMY RESERVOIR WITH OR WITHOUT FILTER
K904566 NEW COBE CENTRYSYSTEM(TM) 100 HG DIALYZER
K902758 COBE SATURATION/HEMATOCRIT MONITOR W/ FIBER OPTIC
K902759 COBE CLOSED WOUND DRAINAGE KIT
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