Alinity i STAT High Sensitivity Troponin-I
FDA 510(k) K230994 · Abbott Laboratories Diagnostics Division
510(k) numberK230994
Submission
- Device name
- Alinity i STAT High Sensitivity Troponin-I
- Applicant
- Abbott Laboratories Diagnostics Division
Abbott Park, IL, US - Received
- April 7, 2023
- Decision date
- May 4, 2023
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MMI – Immunoassay Method, Troponin Subunit
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.1215
- Specialty
- Clinical Chemistry
Other 510(k)s with product code MMI
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K253051 | i-STAT hs-TnI cartridge with the i-STAT Alinity SystemMMI · Traditional | Abbott Point of Care, Inc. | 06/11/2026SE |
| K252393 | VITROS Immunodiagnostic Products hs Troponin I Reagent PackMMI · Traditional | Ortho-Clinical Diagnostics, Inc. | 10/29/2025SE |
| K243483 | Access hsTnIMMI · Traditional | Beckman Coulter, Inc. | 08/01/2025SE |
| K242870 | Access hsTnIMMI · Traditional | Beckman Coulter, Inc. | 06/16/2025SE |
| K240984 | i-STAT hs-TnI cartridge with the i-STAT 1 SystemMMI · Traditional | Abbott Point of Care, Inc. | 01/03/2025SE |
| K241165 | Atellica® IM High-Sensitivity Troponin I (TnIH)MMI · Traditional | Siemens Healthcare Diagnostics, Inc. | 07/25/2024SE |
| K231974 | PATHFAST®hs-cTnI-IIMMI · Traditional | Phc Corporation | 03/20/2024SE |
| K222881 | Access hsTnIMMI · Traditional | Beckman Coulter, Inc. | 12/18/2023SE |
| K230648 | Access hsTnIMMI · Traditional | Beckman Coulter, Inc. | 12/04/2023SE |
| K202525 | Alinity i STAT High Sensitivity Troponin-IMMI · Traditional | Abbott Laboratories Diagnostics Division | 05/19/2022SE |
More from Abbott Laboratories Diagnostics Division
Questions and answers
When was Alinity i STAT High Sensitivity Troponin-I cleared by the FDA?
Alinity i STAT High Sensitivity Troponin-I (K230994) received a 510(k) decision of Substantially Equivalent on May 4, 2023, 27 days after the submission was received.
What is the product code of K230994?
The FDA product code is MMI – Immunoassay Method, Troponin Subunit, a Class II (moderate risk) device regulated under 21 CFR 862.1215.