Clear Guide CORE CGCORE17
Clear Guide CORE CGCORE17 (CG-CORE17) is a Class II device made by Clear Guide Medical, cleared under FDA 510(k) K141806 on 19 Sep 2014 and listed in FDA GUDID since 7 Oct 2022 (UDI-DI B201CGCORE170), 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 | NumberB201CGCORE170 | Date7 Oct 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK141806 | Date19 Sep 2014 | StatusActive |
Official records
- FDA 510(k) database K141806
Across registries
- FDA 510(k) K141806 decided 19 Sep 2014 Active
- FDA GUDID UDI-DI B201CGCORE170 listed 7 Oct 2022 Listed
Timeline
- Cleared FDA 510(k) K141806
- Listed FDA GUDID B201CGCORE170
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Clear Guide CORE
- Generic name
- Ultrasound imaging system workstation
- Model / Ref / Catalog
- CGCORE17, CG-CORE17
- Primary DI / UDI-DI
- B201CGCORE170
- 510(k) Number
- FDA product code
- IYO
- GMDN term
- Ultrasound imaging system workstation
- Device class
- Class II
- Regulation number
- 892.1560
- GUDID distribution status
- In Commercial Distribution
From the manufacturer
Manufacturer's product page: LUMENA
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