FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

COBE CENTRY 2 VARIABLE CONCENTRATE-18-

K Number: K802895 · Decision Dec 22, 1980
Classifications
1
FEI Numbers
231
Registration Numbers
231
Same Product Code
66
Applicant Total
77
Review Days
35

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Basic Information

Device Name
COBE CENTRY 2 VARIABLE CONCENTRATE-18-
K Number
K802895
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Cobe Laboratories, Inc.
Date Received
November 17, 1980
Decision Date
December 22, 1980
Product Code
KDC
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
KDC Instrument, Surgical, Disposable

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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
Search all 77 clearances from Cobe Laboratories, Inc. →