Phamatech Quickscreen Benzodiazepines Test, Models 9025, 9026, 9027T, 9153T and 9195X
by Phamatech, Inc. 510(k)
Active
510(k) K043167
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK043167 | Date29 Dec 2004 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- JXM
- Device Class
- Class II
- Regulation
- 21 CFR Part 862.3170
- Advisory Committee
- Clinical Toxicology
- FDA Decision
- SESE Substantially Equivalent