MJL
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Eia, Blastomyces Dermatitidis
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 866.3060
- Medical specialty
- Microbiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| PREMIER BLASTOMYCES (K923859) | Meridian Diagnostics, Inc. | 1992-10-05 |
| EPIDURAL CATHETER TRAY (K840201) | Aries Medical, Inc. | 1984-03-02 |
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