LJF
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Device, Antimicrobial Drug Removal
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.2560
- Medical specialty
- Microbiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| BACT/ALERT CSR (K003104) | Organon Teknika Corp. | 2000-10-20 |
| ARTIMICROBIAL REMOVAL DEVICE (K830372) | Marion Laboratories, Inc. | 1983-04-08 |
| BACTEC 170 TRYPTIC SOY BROTH W/RESINS (K830363) | Bd Becton Dickinson Vacutainer Systems Preanalytic | 1983-03-24 |
| ANTIMICROBIAL REMOVAL DEVICE (ARD) (K822344) | Marion Laboratories, Inc. | 1982-08-25 |
Track LJF automatically
Every clearance here is in the API, with alerts when new ones post.