Hma Uric Acid Test

FDA 510(k) K781004 · Hycel, Inc.

Substantially Equivalent

510(k) numberK781004

Submission

Device name
Hma Uric Acid Test
Applicant
Hycel, Inc.
Mchenry, IL, US
Received
June 16, 1978
Decision date
July 27, 1978
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

More from A.P. Total Care, Inc.

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K802422Hycel Trigyceride II Test · Traditional 10/06/1980SESP
K790335Hycel MJJF · Traditional 02/27/1979SE
K782176Hycel Ldh-Int TestCFH · Traditional 01/26/1979SE
K782116Ketosteroid Test, HYCEL-17CCY · Traditional 01/26/1979SE
K782102Hycel Counter 211GKL · Traditional 01/03/1979SE
K782101Hycel Counter 222GKL · Traditional 01/03/1979SE
K782100Hycel Counter 333GKL · Traditional 01/03/1979SE
K780946Royco Model 970 Hematology Data AnalyzerJPJ · Traditional 07/27/1978SE
K780464Lelective Kinetic SYSTEM-60JJE · Traditional 05/03/1978SE
K780262Direct Urea Nitrogen TestCDW · Traditional 04/05/1978SE

Questions and answers

When was Hma Uric Acid Test cleared by the FDA?

Hma Uric Acid Test (K781004) received a 510(k) decision of Substantially Equivalent on July 27, 1978, 41 days after the submission was received.

What is the product code of K781004?

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