Trinity Biotech 617739
Trinity Biotech 617739 is a Class II device made by Clark Laboratories, Inc., cleared under FDA 510(k) K920702 on 8 Jul 1992 and listed in FDA GUDID since 26 Dec 2019 (UDI-DI 05391516746823), 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 | Number05391516746823 | Date26 Dec 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK920702 | Date8 Jul 1992 | StatusActive |
Official records
- AccessGUDID record 05391516746823
- FDA 510(k) database K920702
Across registries
- FDA 510(k) K920702 decided 8 Jul 1992 Active
- FDA GUDID UDI-DI 05391516746823 listed 26 Dec 2019 Listed
Timeline
- Cleared FDA 510(k) K920702
- Listed FDA GUDID 05391516746823
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- Withdrawn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
- 617739
- Primary DI / UDI-DI
- 05391516746823
- 510(k) Number
- FDA product code
- LGD
- GMDN term
- Buffered sample diluent IVD, manual
- Device class
- Class II
- Regulation number
- 866.3780
- GUDID distribution status
- In Commercial Distribution
- Size
- Total Volume — 45 Milliliter
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