Lccs S-505-20-Lc
Lccs S-505-20-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 17 Nov 2025 (UDI-DI 04895233602369), 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 | Number04895233602369 | Date17 Nov 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK112231 | Date19 Aug 2011 | StatusActive |
Official records
- AccessGUDID record 04895233602369
- FDA 510(k) database K112231
Across registries
- FDA 510(k) K112231 decided 19 Aug 2011 Active
- FDA GUDID UDI-DI 04895233602369 listed 17 Nov 2025 Listed
Timeline
- Cleared FDA 510(k) K112231
- Listed FDA GUDID 04895233602369
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- Withdrawn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
- S-505-20-LC
- Primary DI / UDI-DI
- 04895233602369
- 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
Other devices filed under FDA product code GXI (Probe, Radiofrequency Lesion).
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- Vesta NLT-150-20-10-BB by Stratus Medical LLC
- RCE-E401519 by Boston Scientific Neuromodulation
- Vesta NLT-150-18-10-BB by Stratus Medical LLC
- Disposable Radiofrequency Cannula by Abbott Medical