Synchron Systems Propoxyphene Reagent
by Beckman Instruments, Inc. 510(k)
Active
510(k) K955675
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK955675 | Date9 Feb 1996 | 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- Withdrawn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
- JXN
- Device Class
- Class II
- Regulation
- 21 CFR Part 862.3700
- Advisory Committee
- Clinical Toxicology
- FDA Decision
- SESE Substantially Equivalent