Iqqa-Liver Multimodality Software
510(k) K131498
Iqqa-Liver Multimodality Software is a Class II device made by EDDA Technology, Inc., cleared under FDA 510(k) K131498 on 25 Jul 2013, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK131498 | Date25 Jul 2013 | StatusActive |
Official records
- FDA 510(k) database K131498
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LLZ
- Device class
- Class II
- Regulation
- 21 CFR Part 892.2050
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K131498
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| EDDA TECHNOLOGY IQQA-Liver Multimodality | IQQA-Liver Multimodality | 00868466000213 | — | On the market |
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