Careside Analyzer
FDA 510(k) K980056 · Exigent Diagnostics, Inc.
510(k) numberK980056
Submission
- Device name
- Careside Analyzer
- Applicant
- Exigent Diagnostics, Inc.
Culver City, CA, US - Received
- January 6, 1998
- Decision date
- March 6, 1998
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- JJF – Analyzer, Chemistry, Micro, For Clinical Use
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 862.2170
- Specialty
- Clinical Chemistry
Other 510(k)s with product code JJF
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K052794 | Eti-Max 3000JJF · Traditional | DiaSorin, Inc. | 03/31/2006SE |
| K040332 | Polymedco Spotchem Ez Chemistry AnalyzerJJF · Traditional | Arkray, Inc. | 06/16/2004SE |
| K033734 | Lightcycler Instrument Version 1.2JJF · Traditional | Roche Diagnostics Corp. | 12/17/2003SE |
| K013654 | Precision Systems Analette Chemistry AnalyzerJJF · Traditional | Precision Systems, Inc. | 06/05/2002SE |
| K012966 | Roche Cobas Taqman AnalyzerJJF · Traditional | Roche Molecular Systems, Inc. | 02/01/2002SE |
| K993634 | Careside AnalyzerJJF · Traditional | Careside, Inc. | 12/02/1999SE |
| K973628 | Vitalab Flexor/Vitalab Selectra 2/VITALAB VivaJJF · Traditional | Vital Scientific N.V. | 03/13/1998SE |
| K973177 | Mago Automated Eia ProcessorJJF · Traditional | Diamedix Corp. | 10/09/1997SE |
| K971491 | Synermed Ir 200 Chemistry AnalyzerJJF · Traditional | Synermed, Inc. | 06/26/1997SE |
| K964506 | Roche Cobas Amplicor AnalyzerJJF · Traditional | Roche Molecular Systems, Inc. | 05/21/1997SE |
More from Roche Molecular Systems, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K982118 | Careside AnalyzerCHH · Traditional | 07/24/1998SE |
| K981899 | Careside Hdl-CholesterolLBS · Traditional | 07/14/1998SE |
| K981183 | Careside GlucoseCGA · Traditional | 05/07/1998SE |
| K980043 | Careside CreatinineJFY · Traditional | 03/30/1998SE |
| K980057 | Careside BunCDQ · Traditional | 02/05/1998SE |
| K980042 | Careside Total ProteinCEK · Traditional | 02/04/1998SE |
| K980041 | Careside AlbuminCIX · Traditional | 02/04/1998SE |
| K980055 | Careside GlobulinJGE · Traditional | 01/28/1998SE |
Questions and answers
When was Careside Analyzer cleared by the FDA?
Careside Analyzer (K980056) received a 510(k) decision of Substantially Equivalent on March 6, 1998, 59 days after the submission was received.
What is the product code of K980056?
The FDA product code is JJF – Analyzer, Chemistry, Micro, For Clinical Use, a Class I (low risk) device regulated under 21 CFR 862.2170.