Unipak Uric Acid

FDA 510(k) K771088 · Harleco

Substantially Equivalent

510(k) numberK771088

Submission

Device name
Unipak Uric Acid
Applicant
Harleco
Mchenry, IL, US
Received
June 16, 1977
Decision date
July 21, 1977
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

Other 510(k)s with product code KNK

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K102568Uric Acid Model 3P39KNK · Traditional Abbott Laboratories05/06/2011SE
K062862Olympus Uric Acid Reagent, Model OSR6X98KNK · Traditional Olympus America, Inc.04/06/2007SE
K040467Vitalab Uric Acid ReagentKNK · Traditional Clinical Data, Inc.03/08/2004SE
K031044Atac Pak Uric Acid Reagent and Atac CalibratorKNK · Traditional Clinical Data, Inc.07/15/2003SE
K022096Uric Acid Assay for the Advia Integrated Modular SystemKNK · Traditional Bayer Diagnostics Corp.03/18/2003SE
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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K813042Ultrachem Gluc-Dh Set, Item #65048LFR · Traditional 11/10/1981SE
K813041Ultrazyme-Gt, Item #64959 & 65032JQB · Traditional 11/10/1981SE
K813040Ultrachem Ca, Item #64975CJY · Traditional 11/10/1981SE
K813039Ultrachem E-Chol, Item #65025CHH · Traditional 11/10/1981SE
K813038Ultrachem TP, Item #64974CEK · Traditional 11/10/1981SE
K812594Ultra Zyme Plus Amyl #64982 & 65031CIJ · Traditional 10/02/1981SE

Questions and answers

When was Unipak Uric Acid cleared by the FDA?

Unipak Uric Acid (K771088) received a 510(k) decision of Substantially Equivalent on July 21, 1977, 35 days after the submission was received.

What is the product code of K771088?

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