STA LIATEST D-DI
FDA 510(k) clearance K141144 · decided 2014-09-03
Clearance details
- K-number
- K141144
- Device name
- STA LIATEST D-DI
- Applicant
- Diagnostica Stago
- Decision
- Substantially Equivalent
- Date received
- 2014-05-02
- Decision date
- 2014-09-03
- Days to decision
- 124 days
- Clearance type
- Traditional
- Product code
- DAP
- Device class
- 2
- Regulation number
- 864.7320
- Medical specialty
- Hematology
- Advisory committee
- Hematology
- Location
- Rome, IT
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| HemosIL D-Dimer HS 500 (K172903) | Instrumentation Laboratory CO | 2017-11-22 |
| STA® - Liatest® D-Di (K162227) | Diagnostica Stago | 2016-12-10 |
| HemosIL D-Dimer HS (K160885) | Instrumentation Laboratory CO | 2016-10-27 |
| HemosIL D-Dimer HS (K151534) | Instrumentation Laboratory CO | 2015-07-06 |
| VIDAS D-DIMER EXCLUSION II (DEX2) (K112818) | bioMerieux, Inc. | 2012-07-31 |
| STRATUS CS ACUTE CARE D-DIMER (K110303) | Siemens Healthcare Diagnostics | 2011-05-16 |
| INNOVANCE D-DIMER, MODEL OPBP09 (K093626) | Siemens Healthcare Diagnostics | 2010-11-29 |
| HEMOSIL D-DIMER HS 500, CONTROLS (K090264) | Instrumentation Laboratory CO | 2010-02-05 |
| INNOVANCE D-DIMER, MODEL OPBP09 (K091916) | Siemens Healthcare Diagnostics | 2009-10-29 |
| INNOVANCE D-DIMER AND INNOVANCE D-DIMER CONTROLS (K081732) | Siemens Healthcare Diagnostics | 2008-10-24 |
| HEMOSIL D-DIMER (K073042) | Instrumentation Laboratory | 2008-07-31 |
| DIMERTEST (K080069) | American Diagnostica, Inc. | 2008-02-13 |
Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| Product: STA Liatest D-Di; REF: 00515; recall (Z-0205-2026) | Diagnostica Stago, Inc. | 2025-10-16 |