Vaginal Stim Sensor SA9572
Vaginal Stim Sensor SA9572 is a Class II device made by Thought Technology Ltd., cleared under FDA 510(k) K053434 on 15 Mar 2006 and listed in FDA GUDID since 31 Aug 2017 (UDI-DI 07540191000418), 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 | Number07540191000418 | Date31 Aug 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK053434 | Date15 Mar 2006 | StatusActive |
Official records
- AccessGUDID record 07540191000418
- FDA 510(k) database K053434
Across registries
- FDA 510(k) K053434 decided 15 Mar 2006 Active
- FDA GUDID UDI-DI 07540191000418 listed 31 Aug 2017 Listed
Timeline
- Cleared FDA 510(k) K053434
- Listed FDA GUDID 07540191000418
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Vaginal Stim Sensor
- Generic name
- Physical therapy transcutaneous neuromuscular electrical stimulation system
- Model / reference
- SA9572
- Primary DI / UDI-DI
- 07540191000418
- 510(k) Number
- FDA product code
- HCC, KPI
- GMDN term
- Physical therapy transcutaneous neuromuscular electrical stimulation system
- Device class
- Class II
- Regulation number
- 882.5050, 876.5320
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code HCC (Device, Biofeedback).
- RELAXOMAT by Relaxomat, Inc.
- EEG BIOFEEDBACK DEVICE by Electronics Research & Production
- ALPHAONE BIOFEEDBACK SYSTEM by Telediagnostic Systems, Inc.
- EAR MUFFINS by Bio-Logic Systems Corp.
- GRINDCARE by Medotech A/S
- EMG RETRAINER by Chattanooga Group, Inc.
- CANARY BREATHING SYSTEM by Palo Alto Health Sciences, Inc.
- AUTOMATED THERAPY SYSTEM by Harding & Harris, Inc.
- Mobile Arm Rehabilitation Kit (MARK) MARK 26215 by Myomo, Inc.
- SLEEP MANAGEMENT SYSTEM by Rmp Co.