Rapid Response D5.1-1VF
Rapid Response D5.1-1VF is a Class II device made by BTNX Inc, cleared under FDA 510(k) K180349 on 5 Apr 2018 and listed in FDA GUDID since 4 Aug 2023 (UDI-DI 10722066007560), 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 | Number10722066007560 | Date4 Aug 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK180349 | Date5 Apr 2018 | StatusActive |
Official records
- AccessGUDID record 10722066007560
- FDA 510(k) database K180349
Across registries
- FDA 510(k) K180349 decided 5 Apr 2018 Active
- FDA GUDID UDI-DI 10722066007560 listed 4 Aug 2023 Listed
Timeline
- Cleared FDA 510(k) K180349
- Listed FDA GUDID 10722066007560
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Rapid Response
- Generic name
- Multiple drugs of abuse IVD, kit, rapid ICT, clinical
- Model / reference
- D5.1-1VF
- Primary DI / UDI-DI
- 10722066007560
- 510(k) Number
- FDA product code
- NGL, NFY, NFW, NGG, NFT
- GMDN term
- Multiple drugs of abuse IVD, kit, rapid ICT, clinical
- Device class
- Class II
- Regulation number
- 862.3650, 862.3250, 862.3870, 862.3610, 862.3100
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Multiple drugs of abuse IVD, kit, rapid ICT, clinical.