Clear Guide CORE CGCORE24
Clear Guide CORE CGCORE24 (CG-CORE24) is a Class II device made by Clear Guide Medical, cleared under FDA 510(k) K153004 on 12 Feb 2016 and listed in FDA GUDID since 7 Oct 2022 (UDI-DI B201CGCORE240), 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 | NumberB201CGCORE240 | Date7 Oct 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK153004 | Date12 Feb 2016 | StatusActive |
Official records
- FDA 510(k) database K153004
Across registries
- FDA 510(k) K153004 decided 12 Feb 2016 Active
- FDA GUDID UDI-DI B201CGCORE240 listed 7 Oct 2022 Listed
Timeline
- Cleared FDA 510(k) K153004
- Listed FDA GUDID B201CGCORE240
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- Withdrawn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
- CGCORE24, CG-CORE24
- Primary DI / UDI-DI
- B201CGCORE240
- 510(k) Number
- FDA product code
- JAK
- GMDN term
- Ultrasound imaging system workstation
- Device class
- Class II
- Regulation number
- 892.1750
- GUDID distribution status
- In Commercial Distribution
From the manufacturer
Manufacturer's product page: LUMENA
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