FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

ASPARTATE AMINOTRANSFERASE-SL ASSAY, CATALOGUE NUMBER 319-10, 319-30

K Number: K974001 · Decision Nov 13, 1997
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
138
Applicant Total
66
Review Days
23

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Basic Information

Device Name
ASPARTATE AMINOTRANSFERASE-SL ASSAY, CATALOGUE NUMBER 319-10, 319-30
K Number
K974001
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1100
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Diagnostic Chemicals , Ltd.
Date Received
October 21, 1997
Decision Date
November 13, 1997
Product Code
CIT
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
CIT Nadh Oxidation/Nad Reduction, Ast/Sgot

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K060140 CRP-ADVANCE MULTI CALIBRATOR SET, MODEL SE-250
K051757 CALCIUM ADVANCE ASSAY, MODEL 145-20, 145-25, 145-20-91
K051191 DCL MICROALBUMIN ASSAY, MODEL 252-20
K042330 ACETAMINOPHEN-SL ASSAY
K042329 SALICYLATE-SL ASSAY
K042362 MODIFICATION TO CARBON DIOXIDE-L3K ASSAY, CAT. NOS. 299-30, 299-17, 299-50, 299-80 AND 299-12
K041928 HDL-ADVANCE ASSAY, CAT. NO. 278-20, 278-50A, 278-50B
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