STM9000 Basic B9800086011
by Eb Neuro SpA
STM9000 Basic B9800086011 is a Class II device made by Eb Neuro SpA, cleared under FDA 510(k) K150220 on 19 Aug 2015 and listed in FDA GUDID since 24 May 2019 (UDI-DI 08056446900741), 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 | Number08056446900741 | Date24 May 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK150220 | Date19 Aug 2015 | StatusActive |
Official records
- AccessGUDID record 08056446900741
- FDA 510(k) database K150220
Across registries
- FDA 510(k) K150220 decided 19 Aug 2015 Active
- FDA GUDID UDI-DI 08056446900741 listed 24 May 2019 Listed
Timeline
- Cleared FDA 510(k) K150220
- Listed FDA GUDID 08056446900741
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- STM9000 Basic
- Generic name
- Magnetic neural stimulation system, stationary
- Model / reference
- B9800086011
- Primary DI / UDI-DI
- 08056446900741
- 510(k) Number
- FDA product code
- GWF
- GMDN term
- Magnetic neural stimulation system, stationary
- Device class
- Class II
- Regulation number
- 882.1870
- GUDID distribution status
- In Commercial Distribution
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