Vaginal Sensor Unit TTL SA6050
Vaginal Sensor Unit TTL SA6050 is a Class II device made by Thought Technology Ltd., cleared under FDA 510(k) K932149 on 11 May 1995 and listed in FDA GUDID since 31 Aug 2017 (UDI-DI 07540191000425), 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 | Number07540191000425 | Date31 Aug 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK932149 | Date11 May 1995 | StatusActive |
Official records
- AccessGUDID record 07540191000425
- FDA 510(k) database K932149
Across registries
- FDA 510(k) K932149 decided 11 May 1995 Active
- FDA GUDID UDI-DI 07540191000425 listed 31 Aug 2017 Listed
Timeline
- Cleared FDA 510(k) K932149
- Listed FDA GUDID 07540191000425
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Vaginal Sensor Unit TTL
- Generic name
- Pelvic floor muscle exerciser
- Model / reference
- SA6050
- Primary DI / UDI-DI
- 07540191000425
- 510(k) Number
- FDA product code
- HIR
- GMDN term
- Pelvic floor muscle exerciser
- Device class
- Class II
- Regulation number
- 884.1425
- GUDID distribution status
- In Commercial Distribution
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