Lccs SS2450-Lc
Lccs SS2450-Lc is a Class II device made by Lccs Products Limited, cleared under FDA 510(k) K131006 on 6 Dec 2013 and listed in FDA GUDID since 24 Jul 2021 (UDI-DI 04895233607319), 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 | Number04895233607319 | Date24 Jul 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK131006 | Date6 Dec 2013 | StatusActive |
Official records
- AccessGUDID record 04895233607319
- FDA 510(k) database K131006
Across registries
- FDA 510(k) K131006 decided 6 Dec 2013 Active
- FDA GUDID UDI-DI 04895233607319 listed 24 Jul 2021 Listed
Timeline
- Cleared FDA 510(k) K131006
- Listed FDA GUDID 04895233607319
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Lccs
- Generic name
- Spinal needle, single-use
- Model / reference
- SS2450-LC
- Primary DI / UDI-DI
- 04895233607319
- 510(k) Number
- FDA product code
- BSP
- GMDN term
- Spinal needle, single-use
- Device class
- Class II
- Regulation number
- 868.5150
- GUDID distribution status
- In Commercial Distribution
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