ClosureRFG RFG3
ClosureRFG RFG3 is a Class II device made by Covidien LP, cleared under FDA 510(k) K141858 on 5 Aug 2014 and listed in FDA GUDID since 11 May 2017 (UDI-DI 10884521713444), 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 | Number10884521713444 | Date11 May 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK141858 | Date5 Aug 2014 | StatusActive |
Official records
- AccessGUDID record 10884521713444
- FDA 510(k) database K141858
Across registries
- FDA 510(k) K141858 decided 5 Aug 2014 Active
- FDA GUDID UDI-DI 10884521713444 listed 11 May 2017 Listed
Timeline
- Cleared FDA 510(k) K141858
- Listed FDA GUDID 10884521713444
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- ClosureRFG
- Generic name
- Percutaneous radio-frequency ablation system generator
- Model / reference
- RFG3
- Primary DI / UDI-DI
- 10884521713444
- 510(k) Number
- FDA product code
- GEI
- GMDN term
- Percutaneous radio-frequency ablation system generator
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
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