Careside Analyzer
FDA 510(k) K981610 · Careside, Inc.
510(k) numberK981610
Submission
- Device name
- Careside Analyzer
- Applicant
- Careside, Inc.
Culver City, CA, US - Received
- April 30, 1998
- Decision date
- June 25, 1998
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- CEO – Phosphomolybdate (Colorimetric), Inorganic Phosphorus
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 862.1580
- Specialty
- Clinical Chemistry
Other 510(k)s with product code CEO
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K100263 | Elitech Clinical Systems Phosphorus, Uric Acid Mono SL and Urea UV SL ReagentsCEO · Traditional | Seppim S.A.S. | 05/06/2011SE |
| K072141 | S40 Clinical Analyzer, S Test Ip, S Test UaCEO · Traditional | Alfa Wassermann Diagnostic Technologies, Inc. | 06/24/2008SE |
| K041643 | Synchron Systems Phosphorus (PHS) ReagentCEO · Traditional | Beckman Coulter, Inc. | 08/18/2004SE |
| K030015 | Atac Pak Phosphorus ReagentCEO · Traditional | Elan Diagnostics | 03/07/2003SE |
| K022312 | Piccolo Phosphorus Test SystemCEO · Traditional | Abaxis, Inc. | 09/05/2002SE |
| K013095 | Wiener Lab.Fosfatemia UV, Models 1X100 ML Cat.N 1382321, 4X20 ML Cat.N 1009311CEO · Traditional | Wiener Laboratories Saic | 11/16/2001SE |
| K003912 | Phosphorus ReagentCEO · Traditional | Jas Diagnostics, Inc. | 02/21/2001SE |
| K003012 | Raichem Phosporus ReagentCEO · Special | Hemagen Diagnostics, Inc. | 10/25/2000SE |
| K991867 | Inorganic Phosphorus (Ip), Product No's, 112-01, 112-02CEO · Traditional | A.P. Total Care, Inc. | 08/02/1999SE |
| K983503 | Roche Diagnostics, Boehringer Mannheim Corporation Inorganic Phosphorus Reagent Catalog…CEO · Traditional | Boehringer Mannheim Corp. | 12/01/1998SE |
More from Boehringer Mannheim Corp.
| 510(k) | Device | Decision |
|---|---|---|
| K020484 | Careside LDHCFH · Traditional | 07/03/2002SE |
| K020486 | Careside GGTJPZ · Traditional | 07/01/2002SE |
| K020487 | Careside AltCKA · Traditional | 06/04/2002SE |
| K020488 | Careside TrglycerideCDT · Traditional | 04/15/2002SE |
| K002792 | Careside CholinesteraseDIH · Traditional | 11/08/2000SE |
| K001462 | Careside HemoglobinKHG · Traditional | 08/21/2000SE |
| K993771 | Careside Direct BilirubinCIG · Traditional | 12/27/1999SE |
| K993634 | Careside AnalyzerJJF · Traditional | 12/02/1999SE |
| K992475 | Careside CO2, TotalKHS · Traditional | 09/15/1999SE |
| K991717 | Careside MGJGJ · Traditional | 08/10/1999SE |
Questions and answers
When was Careside Analyzer cleared by the FDA?
Careside Analyzer (K981610) received a 510(k) decision of Substantially Equivalent on June 25, 1998, 56 days after the submission was received.
What is the product code of K981610?
The FDA product code is CEO – Phosphomolybdate (Colorimetric), Inorganic Phosphorus, a Class I (low risk) device regulated under 21 CFR 862.1580.