Uric Acid Reagent Set
FDA 510(k) K880277 · Tech-Neal Scientific, Inc.
510(k) numberK880277
Submission
- Device name
- Uric Acid Reagent Set
- Applicant
- Tech-Neal Scientific, Inc.
Westmont, IL, US - Received
- January 21, 1988
- Decision date
- April 18, 1988
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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) | Device | Applicant | Decision |
|---|---|---|---|
| K102568 | Uric Acid Model 3P39KNK · Traditional | Abbott Laboratories | 05/06/2011SE |
| K062862 | Olympus Uric Acid Reagent, Model OSR6X98KNK · Traditional | Olympus America, Inc. | 04/06/2007SE |
| K040467 | Vitalab Uric Acid ReagentKNK · Traditional | Clinical Data, Inc. | 03/08/2004SE |
| K031044 | Atac Pak Uric Acid Reagent and Atac CalibratorKNK · Traditional | Clinical Data, Inc. | 07/15/2003SE |
| K022096 | Uric Acid Assay for the Advia Integrated Modular SystemKNK · Traditional | Bayer Diagnostics Corp. | 03/18/2003SE |
| K023550 | Wiener Lab Uricostat Enzimatico Aa LiquidaKNK · Traditional | Wiener Laboratories Saic | 12/09/2002SE |
| K012038 | Jas Uric Acid Liquid ReagentKNK · Traditional | Jas Diagnostics, Inc. | 08/21/2001SE |
| K010421 | Wiener Lab. Uricostat Enzimatico Aa, Models 2X50 ML Catalogue No 1840106 and 4X50 ML…KNK · Traditional | Wiener Laboratories Saic | 04/13/2001SE |
| K993469 | Wako L-Type Ua F TestKNK · Traditional | Wako Chemicals USA, Inc. | 11/09/1999SE |
| K991247 | Uric Acid, Model UA112-01KNK · Traditional | A.P. Total Care, Inc. | 05/25/1999SE |
More from A.P. Total Care, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K882256 | Magnesium Reagent SetJGJ · Traditional | 08/08/1988SE |
| K882459 | Diazo, Colorimetric BilirubinCIG · Traditional | 08/02/1988SE |
| K881239 | Gamma Glutamyl Transferase Reagent SetJPZ · Traditional | 05/31/1988SE |
| K881241 | Total Bilirubin ReagentCIG · Traditional | 05/27/1988SE |
| K881240 | Chloride Reagent SetCHJ · Traditional | 04/28/1988SE |
| K881237 | Creatine Kinase (CK) Reagent SetJHX · Traditional | 04/28/1988SE |
| K880237 | CholesterolCHH · Traditional | 04/28/1988SE |
| K880845 | Calcium Reagent SetCIC · Traditional | 04/05/1988SE |
| K880844 | Albumin Reagent SetCIX · Traditional | 04/05/1988SE |
| K880843 | Creatinine Reagent Set (Kinetic)CGX · Traditional | 04/05/1988SE |
Questions and answers
When was Uric Acid Reagent Set cleared by the FDA?
Uric Acid Reagent Set (K880277) received a 510(k) decision of Substantially Equivalent on April 18, 1988, 88 days after the submission was received.
What is the product code of K880277?
The FDA product code is KNK – Acid, Uric, Uricase (Colorimetric), a Class I (low risk) device regulated under 21 CFR 862.1775.