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

CREATINE KINASE (CK) REAGENT SET

K Number: K881237 · Decision Apr 28, 1988
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
47
Applicant Total
20
Review Days
37

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Basic Information

Device Name
CREATINE KINASE (CK) REAGENT SET
K Number
K881237
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Tech-Neal Scientific, Inc.
Date Received
March 22, 1988
Decision Date
April 28, 1988
Product Code
JHX
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
JHX Fluorometric Method, Cpk Or Isoenzymes

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Other Clearances by Tech-Neal Scientific, Inc.

K Number Device Name
K882256 MAGNESIUM REAGENT SET
K882459 DIAZO, COLORIMETRIC BILIRUBIN
K881239 GAMMA GLUTAMYL TRANSFERASE REAGENT SET
K881241 TOTAL BILIRUBIN REAGENT
K880237 CHOLESTEROL
K881240 CHLORIDE REAGENT SET
K880277 URIC ACID REAGENT SET
K880845 CALCIUM REAGENT SET
K880842 LDH-L REAGENT SET
K880844 ALBUMIN REAGENT SET
Search all 20 clearances from Tech-Neal Scientific, Inc. →