Trinity Biotech 616474
Trinity Biotech 616474 is a buffered sample diluent IVD (FDA Class II; FDA product code LSR, Reagent, Borrelia Serological Reagent) made by Clark Laboratories, Inc., cleared under FDA 510(k) K033083 on 26 Nov 2003 and listed in FDA GUDID since 26 Dec 2019 (UDI-DI 05391516746779), 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 | Number05391516746779 | Date26 Dec 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK033083 | Date26 Nov 2003 | StatusActive |
Official records
- AccessGUDID record 05391516746779
- FDA 510(k) database K033083
Across registries
- FDA 510(k) K033083 decided 26 Nov 2003 Active
- FDA GUDID UDI-DI 05391516746779 listed 26 Dec 2019 Listed
Timeline
- Cleared FDA 510(k) K033083
- Listed FDA GUDID 05391516746779
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Trinity Biotech
- Generic name
- Buffered sample diluent IVD, manual
- Model / reference
- 616474
- Primary DI / UDI-DI
- 05391516746779
- 510(k) Number
- FDA product code
- LSR
- GMDN term
- Buffered sample diluent IVD, manual
- Device class
- Class II
- Regulation number
- 866.3830
- GUDID distribution status
- In Commercial Distribution
- Size
- Total Volume — 30 Milliliter
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