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

COULTER GLUCOSE REAGENT

K Number: K897160 · Decision Mar 9, 1990
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
144
Applicant Total
101
Review Days
71

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Basic Information

Device Name
COULTER GLUCOSE REAGENT
K Number
K897160
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1345
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Coulter Electronics, Inc.
Date Received
December 28, 1989
Decision Date
March 9, 1990
Product Code
CFR
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
CFR Hexokinase, Glucose

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K923530 COULTER MULTI-Q-PREP
K922181 COULTER MH009
K922704 COULTER MAXM W/ AUTOLOADER
K921567 COULTER MH017
K912133 PX COULTER(R) CELL CONTROL
K911385 COULTER(R) MH010
K905771 COULTER DART AST (GOT) REAGENT
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