Thd Slide One
by Thd SpA
510(k) K090009
Thd Slide One is a Class II device made by Thd SpA, cleared under FDA 510(k) K090009 on 28 Jan 2009, 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 | NumberK090009 | Date28 Jan 2009 | StatusActive |
Official records
- FDA 510(k) database K090009
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- JAF
- Device class
- Class II
- Regulation
- 21 CFR Part 892.1540
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K090009
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 | |||
|---|---|---|---|---|
| THD Revolution THD Slide One USA | 800070 / THD Slide One USA | 08033737710739 | On the market | |
| THD SLIDE ONE | 710004 / THD SLIDE | 08033737710869 | On the market | |
| THD SLIDE ONE THD ANOLIFT US | 800330 / THD ANOLIFT US | 08051887047918 | On the market | |
| THD SLIDE ONE THD DOPPLER PROBE (1s/ST) | 800063 / THD DOPPLER PROBE (1s/ST) | 18033737710354 | On the market | |
| THD SLIDE ONE THD OPTI-FIBER (EVO/BT) | 880018 / THD OPTI-FIBER (EVO/BT) | 18033737710781 | On the market | |
| THD SLIDE ONE THD OPTI-FIBER (REVO/BT) | 880012 / THD OPTI-FIBER (REVO/BT) | 08033737710777 | On the market |
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