Careside Analyzer
FDA 510(k) K982118 · Exigent Diagnostics, Inc.
510(k) numberK982118
Submission
- Device name
- Careside Analyzer
- Applicant
- Exigent Diagnostics, Inc.
Culver City, CA, US - Received
- June 3, 1998
- Decision date
- July 24, 1998
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- CHH – Enzymatic Esterase--Oxidase, Cholesterol
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 862.1175
- Specialty
- Clinical Chemistry
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| K251091 | LipidsCHH · Traditional | Truvian Health | 12/30/2025SE |
| K232404 | CHOLESTEROL; HDL-cholesterol ; LDL-cholesterol; TRIGLYCERIDESCHH · Traditional | Medicon Hellas S.A | 08/09/2024SE |
| K203597 | Cholesterol2CHH · Traditional | Abbott Ireland Diagnostics Division | 06/30/2022SE |
| K190490 | VITROS XT Chemistry Products TRIG-CHOL SlidesCHH · Traditional | Ortho-Clinical Diagnostics, Inc. | 03/27/2019SE |
| K181373 | Extended Lipid Panel AssayCHH · Traditional | Laboratory Corporation of America Holdings | 10/18/2018SE |
| K180504 | Mission Lipid Panel Monitoring SystemCHH · Special | ACON Laboratories, Inc. | 03/28/2018SE |
| K163406 | Mission Cholesterol Monitoring System, Mission Cholesterol Pro Monitoring SystemCHH · Traditional | ACON Laboratories, Inc. | 07/11/2017SE |
| K151545 | CardioChek Plus Test System, CardioChek Home Test System, CardioChek PA Test System…CHH · Traditional | Polymer Technology Systems, Inc. | 12/22/2016SE |
| K150654 | CholesterolCHH · Traditional | Randox Laboratories, Ltd. | 09/29/2015SE |
| K132031 | Afinion Lipid Panel and Afinion Lipid Panel ControlCHH · Traditional | Axis-Shield Poc AS | 03/21/2014SE |
More from Axis-Shield Poc AS
| 510(k) | Device | Decision |
|---|---|---|
| K981899 | Careside Hdl-CholesterolLBS · Traditional | 07/14/1998SE |
| K981183 | Careside GlucoseCGA · Traditional | 05/07/1998SE |
| K980043 | Careside CreatinineJFY · Traditional | 03/30/1998SE |
| K980056 | Careside AnalyzerJJF · Traditional | 03/06/1998SE |
| 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 (K982118) received a 510(k) decision of Substantially Equivalent on July 24, 1998, 51 days after the submission was received.
What is the product code of K982118?
The FDA product code is CHH – Enzymatic Esterase--Oxidase, Cholesterol, a Class I (low risk) device regulated under 21 CFR 862.1175.