ElectrodeCRF CRF-N2035
by Cambridge Interventional LLC
ElectrodeCRF CRF-N2035 is a Class II device made by Cambridge Interventional LLC, cleared under FDA 510(k) K192715 on 7 Jan 2020 and listed in FDA GUDID since 30 Apr 2020 (UDI-DI 00811746031186), 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 | Number00811746031186 | Date30 Apr 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK192715 | Date7 Jan 2020 | StatusActive |
Official records
- AccessGUDID record 00811746031186
- FDA 510(k) database K192715
Across registries
- FDA 510(k) K192715 decided 7 Jan 2020 Active
- FDA GUDID UDI-DI 00811746031186 listed 30 Apr 2020 Listed
Timeline
- Cleared FDA 510(k) K192715
- Listed FDA GUDID 00811746031186
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- ElectrodeCRF
- Generic name
- Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar
- Model / Ref / Catalog
- CRF-N2035
- Primary DI / UDI-DI
- 00811746031186
- 510(k) Number
- FDA product code
- GEI
- GMDN term
- Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
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