Lccs C-1010-18-Lc
Lccs C-1010-18-Lc is a Class II device made by Lccs Products Limited, cleared under FDA 510(k) K112231 on 19 Aug 2011 and listed in FDA GUDID since 24 Jul 2021 (UDI-DI 04895233601720), 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 | Number04895233601720 | Date24 Jul 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK112231 | Date19 Aug 2011 | StatusActive |
Official records
- AccessGUDID record 04895233601720
- FDA 510(k) database K112231
Across registries
- FDA 510(k) K112231 decided 19 Aug 2011 Active
- FDA GUDID UDI-DI 04895233601720 listed 24 Jul 2021 Listed
Timeline
- Cleared FDA 510(k) K112231
- Listed FDA GUDID 04895233601720
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Lccs
- Generic name
- Percutaneous radio-frequency ablation probe cannula, single-use
- Model / reference
- C-1010-18-LC
- Primary DI / UDI-DI
- 04895233601720
- 510(k) Number
- FDA product code
- GXI
- GMDN term
- Percutaneous radio-frequency ablation probe cannula, single-use
- Device class
- Class II
- Regulation number
- 882.4725
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Percutaneous radio-frequency ablation probe cannula, single-use.