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

GLUCOSE-HK REAGENT

K Number: K873835 · Decision Nov 24, 1987
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
144
Applicant Total
21
Review Days
64

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Basic Information

Device Name
GLUCOSE-HK REAGENT
K Number
K873835
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1345
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Intersect Systems, Inc.
Date Received
September 21, 1987
Decision Date
November 24, 1987
Product Code
CFR
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
CFR Hexokinase, Glucose

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Other Clearances by Intersect Systems, Inc.

K Number Device Name
K021636 ALBUMIN REAGENT
K011972 DIRECT BILIRUBIN REAGENT
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
Search all 21 clearances from Intersect Systems, Inc. →