FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇪 Ireland

CK-MB (NAC-ACT)

K Number: K951223 · Decision Dec 26, 1995
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
122
Applicant Total
116
Review Days
281

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Basic Information

Device Name
CK-MB (NAC-ACT)
K Number
K951223
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Randox Laboratories, Ltd.
Date Received
March 20, 1995
Decision Date
December 26, 1995
Product Code
CGS
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
CGS Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes

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