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

ENZYMATIC CREATININE ASSAY (265 SERIES)

K Number: K070383 · Decision Jun 22, 2007
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
48
Applicant Total
66
Review Days
133

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Basic Information

Device Name
ENZYMATIC CREATININE ASSAY (265 SERIES)
K Number
K070383
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1225
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Diagnostic Chemicals , Ltd.
Date Received
February 9, 2007
Decision Date
June 22, 2007
Product Code
JFY
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
JFY Enzymatic Method, Creatinine

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Other Clearances by Diagnostic Chemicals , Ltd.

K Number Device Name
K063208 MAGNESIUM ASSAY (XB), MODELS 125-12, 125-50 AND 125-S7
K060139 CRP-ADVANCE ASSAY, MODELS 250-20, 250-25
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
K041926 HDL/LDL-ADVANCE CALIBRATOR, CAT. NO. SE-278
Search all 66 clearances from Diagnostic Chemicals , Ltd. →