Uricase (U.V.) Uric Acid
FDA 510(k) K821167 · Syn-Kit, Inc.
510(k) numberK821167
Submission
- Device name
- Uricase (U.V.) Uric Acid
- Applicant
- Syn-Kit, Inc.
Mchenry, IL, US - Received
- April 27, 1982
- Decision date
- May 14, 1982
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- CDO – Acid, Uric, Uricase (U.V.)
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 862.1775
- Specialty
- Clinical Chemistry
Other 510(k)s with product code CDO
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K033278 | Randox Uric AcidCDO · Traditional | Randox Laboratories, Ltd. | 02/27/2004SE |
| K992798 | Sigma Diagnostics Infinity Uric Acid Reagent, Models 684-25, 684-100P, 684-500P…CDO · Traditional | Sigma Diagnostics, Inc. | 09/28/1999SE |
| K982251 | Sigma Diagnostics Infinity Uric Acid Reagent KitCDO · Traditional | Sigma Diagnostics, Inc. | 08/18/1998SE |
| K981766 | Uric AcidCDO · Traditional | Abbott Laboratories | 06/19/1998SE |
| K981189 | Uric AcidCDO · Traditional | Abbott Laboratories | 05/07/1998SE |
| K971485 | Uric Acid - Incorporating Dynamic Stabilization Technology - (DST)CDO · Traditional | Trace America, Inc. | 05/27/1997SE |
| K955752 | Olympus Uric Acid ReagentCDO · Traditional | Olympus America, Inc. | 01/31/1996SE |
| K932162 | Uric Acid Test Item Number 65422CDO · Traditional | Em Diagnostic Systems, Inc. | 09/27/1993SE |
| K923765 | Systemate Uricacid Test, Technicon Ra 1000CDO · Traditional | Em Diagnostic Systems, Inc. | 09/22/1992SE |
| K903335 | Systemate Uric Acid (Urca) Item Number 65422CDO · Traditional | Em Diagnostic Systems, Inc. | 08/17/1990SE |
More from Em Diagnostic Systems, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K861098 | Seroiden Strepto Kit 'Eiken'GTZ · Traditional | 08/12/1986SE |
| K861631 | Slide Culture U 'Eiken'JXA · Traditional | 06/10/1986SE |
| K854819 | CPR Slide EikenDCN · Traditional | 02/26/1986SE |
| K854820 | Ra 80 EikenDHR · Traditional | 01/17/1986SE |
| K853276 | Aso Slide EikenGTQ · Traditional | 08/20/1985SE |
| K843760 | Uropaper Eiken GJIL · Traditional | 12/18/1984SE |
| K843759 | Uropaper Eiken HagJIL · Traditional | 12/18/1984SE |
| K843758 | Uropaper Eiken GKJIL · Traditional | 12/18/1984SE |
| K843757 | Uropaper Eiken AGJIL · Traditional | 12/18/1984SE |
| K843756 | Uropaper Eiken 5JIL · Traditional | 12/18/1984SE |
Questions and answers
When was Uricase (U.V.) Uric Acid cleared by the FDA?
Uricase (U.V.) Uric Acid (K821167) received a 510(k) decision of Substantially Equivalent on May 14, 1982, 17 days after the submission was received.
What is the product code of K821167?
The FDA product code is CDO – Acid, Uric, Uricase (U.V.), a Class I (low risk) device regulated under 21 CFR 862.1775.