Uric Acid REAGENT-ENZYMATIC-COLOR-520 NM

FDA 510(k) K812641 · Reagents Applications, Inc.

Substantially Equivalent

510(k) numberK812641

Submission

Device name
Uric Acid REAGENT-ENZYMATIC-COLOR-520 NM
Applicant
Reagents Applications, Inc.
Mchenry, IL, US
Received
September 16, 1981
Decision date
October 2, 1981
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KNK – Acid, Uric, Uricase (Colorimetric)
Device class
Class I (low risk)
Regulation
21 CFR 862.1775
Specialty
Clinical Chemistry

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K023550Wiener Lab Uricostat Enzimatico Aa LiquidaKNK · Traditional Wiener Laboratories Saic12/09/2002SE
K012038Jas Uric Acid Liquid ReagentKNK · Traditional Jas Diagnostics, Inc.08/21/2001SE
K010421Wiener Lab. Uricostat Enzimatico Aa, Models 2X50 ML Catalogue No 1840106 and 4X50 ML…KNK · Traditional Wiener Laboratories Saic04/13/2001SE
K993469Wako L-Type Ua F TestKNK · Traditional Wako Chemicals USA, Inc.11/09/1999SE
K991247Uric Acid, Model UA112-01KNK · Traditional A.P. Total Care, Inc.05/25/1999SE

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K911898Raichem(Tm) Spia(Tm) Haptoglobin ReagentDAD · Traditional 05/08/1991SE
K905085Raichem GGT ReagentJQB · Traditional 12/20/1990SE
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Questions and answers

When was Uric Acid REAGENT-ENZYMATIC-COLOR-520 NM cleared by the FDA?

Uric Acid REAGENT-ENZYMATIC-COLOR-520 NM (K812641) received a 510(k) decision of Substantially Equivalent on October 2, 1981, 16 days after the submission was received.

What is the product code of K812641?

The FDA product code is KNK – Acid, Uric, Uricase (Colorimetric), a Class I (low risk) device regulated under 21 CFR 862.1775.