THD Procto Software System THD DIGITAL MOBILE ADVANCED
by Thd SpA
THD Procto Software System THD DIGITAL MOBILE ADVANCED (800309) is an ultrasound imaging system application software (FDA Class II) made by Thd SpA, cleared under FDA 510(k) K211623 on 24 Jun 2021 and listed in FDA GUDID since 14 Dec 2023 (UDI-DI 68051887043325), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number68051887043325 | Date14 Dec 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK211623 | Date24 Jun 2021 | StatusActive |
Official records
- AccessGUDID record 68051887043325
- FDA 510(k) database K211623
Across registries
- FDA 510(k) K211623 decided 24 Jun 2021 Active
- FDA GUDID UDI-DI 68051887043325 listed 14 Dec 2023 Listed
Timeline
- Cleared FDA 510(k) K211623
- Listed FDA GUDID 68051887043325
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- THD Procto Software System
- Generic name
- Ultrasound imaging system application software
- Model / Ref / Catalog
- THD DIGITAL MOBILE ADVANCED, 800309
- Primary DI / UDI-DI
- 68051887043325
- 510(k) Number
- FDA product code
- IYO, KLA, ITX, FWG, OUG
- GMDN term
- Ultrasound imaging system application software
- Device class
- Class II
- Regulation number
- 892.1560, 876.1725, 892.1570, 878.4160, 880.6310
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Ultrasound imaging system application software.