CT1896B
CT1896B is a Class II device made by Oxoid Limited, cleared under FDA 510(k) K982523 on 9 Sep 1998 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 05032384184842), active as of 22 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 | Number05032384184842 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK982523 | Date9 Sep 1998 | StatusActive |
Official records
- AccessGUDID record 05032384184842
- FDA 510(k) database K982523
Across registries
- FDA 510(k) K982523 decided 9 Sep 1998 Active
- FDA GUDID UDI-DI 05032384184842 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K982523
- Listed FDA GUDID 05032384184842
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Nafcillin susceptibility testing disc IVD
- Model / reference
- CT1896B
- Primary DI / UDI-DI
- 05032384184842
- 510(k) Number
- FDA product code
- JTN
- GMDN term
- Nafcillin susceptibility testing disc IVD
- Device class
- Class II
- Regulation number
- 866.1620
- GUDID distribution status
- In Commercial Distribution
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