FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

GAMMA GLUTAMYLTRANSFERASE REAGENT

K Number: K871979 · Decision Jun 11, 1987
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
32
Applicant Total
21
Review Days
20

Basic Information

Device Name
GAMMA GLUTAMYLTRANSFERASE REAGENT
K Number
K871979
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1360
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
INTERSECT SYSTEMS, INC.
Date Received
May 22, 1987
Decision Date
June 11, 1987
Product Code
JPZ
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
JPZ Colorimetric Method, Gamma-Glutamyl Transpeptidase

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Other Clearances by INTERSECT SYSTEMS, INC.

K Number Device Name
K021636 ALBUMIN REAGENT
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K011692 HOMOGENEOUS ENZYMIC HOMOCYSTEINE REAGENT
K003892 TOTAL BILIRUBIN REAGENT
K983937 DUAL VIAL CREATININE REAGENT
K974833 CK-NAC REAGENT
K941807 INTERSECT SYSTEMS' NON-MERCURIC CHLORIDE REAGENT
K932888 INTERSECT SYSTEMS DIRECT AMYLASE REAGENT
K934039 INTERSECT SYSTEMS HDL CHOLESTEROL REAGENT SET
K932267 ENZYMATIC CO2 REAGENT, MODIFICATION
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