Convex probe C3S-D
by CHISON Medical Technologies Co., Ltd.
Convex probe C3S-D is a Class II device made by CHISON Medical Technologies Co., Ltd., cleared under FDA 510(k) K162172 on 14 Sep 2016 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 06945121409896), 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 | Number06945121409896 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK162172 | Date14 Sep 2016 | StatusActive |
Official records
- AccessGUDID record 06945121409896
- FDA 510(k) database K162172
Across registries
- FDA 510(k) K162172 decided 14 Sep 2016 Active
- FDA GUDID UDI-DI 06945121409896 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K162172
- Listed FDA GUDID 06945121409896
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Convex probe
- Generic name
- Extracorporeal ultrasound imaging transducer, hand-held
- Model / reference
- C3S-D
- Primary DI / UDI-DI
- 06945121409896
- 510(k) Number
- FDA product code
- ITX
- GMDN term
- Extracorporeal ultrasound imaging transducer, hand-held
- Device class
- Class II
- Regulation number
- 892.1570
- GUDID distribution status
- In Commercial Distribution
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