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

URIC ACID REAGENT SET

K Number: K914158 · Decision Feb 21, 1992
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
117
Applicant Total
13
Review Days
157

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Basic Information

Device Name
URIC ACID REAGENT SET
K Number
K914158
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1775
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Tech Intl. Co.
Date Received
September 17, 1991
Decision Date
February 21, 1992
Product Code
KNK
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
KNK Acid, Uric, Uricase (Colorimetric)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KNK), ordered by most recent decision date.

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Other Clearances by Tech Intl. Co.

K Number Device Name
K915704 AMYLASE (KINETIC) REAGENT SET
K915705 ACID PHOSPHATASE REAGENT SET
K915707 AMMONIA REAGENT SET
K915706 LIPASE REAGENT SET
K915710 AMYLASE (COLORIMETRIC) REAGENT SET
K914160 CHOLESTEROL REGEANT SET
K915709 CREATINE KINASE-MB (CK-MB) REAGENT SET
K914159 GLUCOSE REAGENT SET
K915708 INORGANIC PHOSPHORUS(COLORIMETRIC) REAGENT SET
K914171 IN VITRO DIAGNOSTIC REGEANT SET,CHOLINESTERASE
Search all 13 clearances from Tech Intl. Co. →