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

CREATINKINETIC

K Number: K863079 · Decision Dec 12, 1986
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
158
Applicant Total
34
Review Days
122

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Basic Information

Device Name
CREATINKINETIC
K Number
K863079
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1225
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
J. D. Assoc.
Date Received
August 12, 1986
Decision Date
December 12, 1986
Product Code
CGX
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
CGX Alkaline Picrate, Colorimetry, Creatinine

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CGX), ordered by most recent decision date.

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Other Clearances by J. D. Assoc.

K Number Device Name
K863103 PEG 6,000
K863054 AST S.C.E. (GOT)
K863069 MAGNESIOMETER
K863112 PROTEINMETER
K863068 LDH S.C.E.
K863053 ALT S.C.E. (GPT)
K863066 TRANSFERMETER
K863109 FERROFAST
K863102 GLUCOMETER-E
K863056 BILIRUBIN TOTAL
Search all 34 clearances from J. D. Assoc. →