Bladder Scanner M2-W
by Suzhou PeakSonic Medical Technology Co., LTD.
Bladder Scanner M2-W is a Class II device made by Suzhou PeakSonic Medical Technology Co., LTD., cleared under FDA 510(k) K190769 on 22 May 2019 and listed in FDA GUDID since 19 Jul 2022 (UDI-DI 06975124100285), 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 | GUDID listing | Number06975124100285 | Date19 Jul 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK190769 | Date22 May 2019 | StatusActive |
Official records
- AccessGUDID record 06975124100285
- FDA 510(k) database K190769
Across registries
- FDA 510(k) K190769 decided 22 May 2019 Active
- FDA GUDID UDI-DI 06975124100285 listed 19 Jul 2022 Listed
Timeline
- Cleared FDA 510(k) K190769
- Listed FDA GUDID 06975124100285
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Bladder Scanner
- Generic name
- Bladder volume ultrasound imaging system
- Model / reference
- M2-W
- Primary DI / UDI-DI
- 06975124100285
- 510(k) Number
- FDA product code
- ITX, IYO
- GMDN term
- Bladder volume ultrasound imaging system
- Device class
- Class II
- Regulation number
- 892.1570, 892.1560
- GUDID distribution status
- In Commercial Distribution
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