Emit-Tox Serum Tricyclic Antidepr. Assay
by Syva Co. 510(k)
Active
510(k) K821743
Regulatory status
Recall ongoing. 1 ongoing FDA recall. See recalls
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK821743 | Date2 Jul 1982 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Recalls
-
- Ongoing Z-2881-2026
out-of-specification sodium azide concentration in Syva Emit Tox Serum Tricyclic Antidepressant Calibrator/Controls Lot U2. While the assay results were not impacted, the overall health risk to lab technicians due to this issue is low, as exposure is limited by small volumes and a 0.2% post-reconstitution sodium azide concentration, with the worst outcome being mild skin or eye irritation and no serious harm anticipated.
Specification
- 510(k) Number
- FDA Product Code
- LFG
- Device Class
- Class II
- Regulation
- 21 CFR Part 862.3910
- Advisory Committee
- Clinical Toxicology
- FDA Decision
- SESE Substantially Equivalent