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

URIC ACID, BOUND ENZYME

K Number: K790092 · Decision Mar 12, 1979
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
117
Applicant Total
157
Review Days
55

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Basic Information

Device Name
URIC ACID, BOUND ENZYME
K Number
K790092
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1775
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Technicon Instruments Corp.
Date Received
January 16, 1979
Decision Date
March 12, 1979
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)

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