PhoeniX
510(k) K192011
PhoeniX is a medical device (FDA Class II; FDA product code IZL, System, X-Ray, Mobile) made by Sedecal., Sa., cleared under FDA 510(k) K192011 on 25 Sep 2019, 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 | NumberK192011 | Date25 Sep 2019 | StatusActive |
Official records
- FDA 510(k) database K192011
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- IZL
- Device class
- Class II
- Regulation
- 21 CFR Part 892.1720
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K192011
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 | |||
|---|---|---|---|---|
| SEDECAL ODYSSEY | 2420 / ODYSSEY | 08436046003651 | — | On the market |
| SEDECAL ODYSSEY | 2432 / ODYSSEY | 08436046003668 | — | On the market |
| SEDECAL ODYSSEY | 2440 / ODYSSEY | 08436046003675 | — | On the market |
| SEDECAL ODYSSEY | 2450 / ODYSSEY | 08436046003682 | — | On the market |
| SEDECAL ODYSSEY+ | 2420 / ODYSSEY+ | 08436046003699 | — | On the market |
| SEDECAL ODYSSEY+ | 2432 / ODYSSEY+ | 08436046003705 | — | On the market |
| SEDECAL ODYSSEY+ | 2440 / ODYSSEY+ | 08436046003712 | — | On the market |
| SEDECAL ODYSSEY+ | 2450 / ODYSSEY+ | 08436046003729 | — | On the market |
| SEDECAL PhoeniX | 1020 / PhoeniX | 08436046002364 | — | On the market |
| SEDECAL PhoeniX | 1032 / PhoeniX | 08436046002470 | — | On the market |
| SEDECAL PhoeniX | 1040 / PhoeniX | 08436046002487 | — | On the market |
| SEDECAL PhoeniX | 1050 / PhoeniX | 08436046002494 | — | On the market |
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