Bun Qvet
FDA 510(k) K943042 · Prisma Systems
510(k) numberK943042
Submission
- Device name
- Bun Qvet
- Applicant
- Prisma Systems
Rome, NY, US - Received
- June 27, 1994
- Decision date
- December 29, 1994
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- CDN – Urease, Photometric, Urea Nitrogen
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.1770
- Specialty
- Clinical Chemistry
Other 510(k)s with product code CDN
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K190326 | VITROS XT Chemistry Products UREA-CREA SlidesCDN · Traditional | Ortho-Clinical Diagnostics, Inc. | 03/14/2019SE |
| K132462 | S Test Reagent Cartridge Bun and S Test Reagent Cartridge CreCDN · Traditional | Hitachi Chemical Diagnostics, Inc. | 10/28/2013SE |
| K123322 | Ace Bun/Urea Reagent, Ace Creatinine Reagent, Ace Uric Acid Reagent, Ace CK ReagentCDN · Traditional | Alfa Wassermann Diagnostics Technologies, LLC | 05/21/2013SE |
| K113389 | Ace CK Reagent,Ace Bun/Urea Reagent,Ace Uric Acid Reagent,Ace Creatinine ReagentCDN · Traditional | Alfa Wassermann Diagnostic Technologies, Inc. | 08/10/2012SE |
| K103615 | Ace Urea Nitrogen Reagent, Calcium-Arseazo Reagent, Creatinine Reagent, Inorganic…CDN · Traditional | Alfa Wassermann Diagnostic Technologies, Inc. | 09/08/2011SE |
| K001885 | Vitros Chemistry Products Bun/Urea Slides and Vitros Chemistry Products Calibrator Kit 1CDN · Special | Ortho-Clinical Diagnostics, Inc. | 07/20/2000SE |
| K972012 | Cholestech Bun/Creatinine Test SystemCDN · Traditional | Cholestech Corp. | 07/24/1997SE |
| K961196 | Ektachem Clinical Chemistry Urea Nitrogen/Urea (Bun/Urea)CDN · Traditional | Johnson & Johnson Clinical Diagnostics, Inc. | 05/15/1996SE |
| K922969 | King Diagnostics Urea Nitrogen ReagentCDN · Traditional | King Diagnostics, Inc. | 10/13/1992SE |
| K914903 | Quickstart Urea NitrogenCDN · Traditional | Em Diagnostic Systems, Inc. | 12/31/1991SE |
More from Em Diagnostic Systems, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K950177 | CK QvetCGS · Traditional | 03/03/1995SE |
| K943027 | Cholesterol QvetCHH · Traditional | 01/27/1995SE |
| K943001 | Magnesium QvetJGJ · Traditional | 12/29/1994SE |
| K942997 | Alkaline Phosphatase (Alkp) QvetCJE · Traditional | 12/29/1994SE |
| K942964 | Lactate Dehydrogenase QvetCFJ · Traditional | 12/29/1994SE |
| K942963 | Glucose QvetCFR · Traditional | 12/29/1994SE |
| K944102 | Ast QvetCIT · Traditional | 12/13/1994SE |
| K943000 | Albumin QvetCIX · Traditional | 12/13/1994SE |
| K943026 | Potassium QvetCEJ · Traditional | 12/09/1994SE |
| K943004 | Total Protein QvetCEK · Traditional | 12/09/1994SE |
Questions and answers
When was Bun Qvet cleared by the FDA?
Bun Qvet (K943042) received a 510(k) decision of Substantially Equivalent on December 29, 1994, 185 days after the submission was received.
What is the product code of K943042?
The FDA product code is CDN – Urease, Photometric, Urea Nitrogen, a Class II (moderate risk) device regulated under 21 CFR 862.1770.