510(k) K790486

FLOZYME* URIC ACID REAGENT by Worthington Diagnostic Systems — Product Code KNK

K790486 is an FDA 510(k) premarket notification submitted by Worthington Diagnostic Systems for the device "FLOZYME* URIC ACID REAGENT". The FDA issued a decision of Substantially Equivalent on April 23, 1979. The device falls under product code KNK (Acid, Uric, Uricase (Colorimetric)), a Class I device regulated under 21 CFR 862.1775. Worthington Diagnostic Systems has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 23, 1979
Date Received
March 12, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Acid, Uric, Uricase (Colorimetric)
Device Class
Class I
Regulation Number
862.1775
Review Panel
CH
Submission Type