Uric Acid Reagent Set Enzymatic

FDA 510(k) K841049 · Medical Specialties, Inc.

Substantially Equivalent

510(k) numberK841049

Submission

Device name
Uric Acid Reagent Set Enzymatic
Applicant
Medical Specialties, Inc.
Mchenry, IL, US
Received
March 12, 1984
Decision date
May 1, 1984
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

510(k)DeviceApplicantDecision
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.

510(k)DeviceDecision
K946201Stand, InfusionFOX · Traditional 04/18/1995SE
K931947CheckpointJPK · Traditional 06/18/1993SE
K926095Refractrol-SpJJX · Traditional 01/26/1993SE
K924926Msi-HctGLK · Traditional 01/07/1993SE
K896566Modified Fox Extra Gram Negative and PositiveJWY · Traditional 02/09/1990SE
K883851Msi-Cal 8KRZ · Traditional 11/22/1988SE
K883850Msi-Cal 16KRZ · Traditional 11/22/1988SE
K883703Msi-Cal 7KRZ · Traditional 11/22/1988SE
K880608Msi-PcGJP · Traditional 03/21/1988SE
K880270Msi-Diff PlusJPK · Traditional 03/01/1988SE

Questions and answers

When was Uric Acid Reagent Set Enzymatic cleared by the FDA?

Uric Acid Reagent Set Enzymatic (K841049) received a 510(k) decision of Substantially Equivalent on May 1, 1984, 50 days after the submission was received.

What is the product code of K841049?

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