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

CPK CLINI GEL KIT

K Number: K791826 · Decision Oct 1, 1979
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
20
Applicant Total
30
Review Days
14

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Basic Information

Device Name
CPK CLINI GEL KIT
K Number
K791826
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Clinical Sciences, Inc.
Date Received
September 17, 1979
Decision Date
October 1, 1979
Product Code
JHT
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
JHT Chromatographic Separation, Cpk Isoenzymes

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K891990 RUBEOLA IGG CLIN-ELISA TEST SYSTEM, CAT. #4600
K883600 EPSTEIN-BARR VIRUS (EBNA-1) IGG CATA. #4550
K883601 EPSTEIN-BARR VIRUS (EBNA-1) IGM CATA. #5550
K874594 TOXOPLASMA IGM CLIN-ELISA(TM) CAT # 5560
K872942 IGM CMV CLIN-ELISA(TM) TEST SYSTEM NUMBER: 5530
K860145 RUBELLA ELISA TEST SYSTEM CATALOG NUMBER: 4540
K860773 TOXOPLASMA IGG CLIN-ELISA TEST KIT CAT. NO. 4560
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