Iqqa-Bodyimaging Software
510(k) K141745
Iqqa-Bodyimaging Software is a Class II device made by Edda Technology, cleared under FDA 510(k) K141745 on 31 Oct 2014, 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 | NumberK141745 | Date31 Oct 2014 | StatusActive |
Official records
- FDA 510(k) database K141745
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- Withdrawn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 K141745
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-BodyImaging | IQQA-BodyImaging | 00868466000220 | — | On the market |
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