LTX
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Discs, Elution
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 866.1620
- Medical specialty
- Microbiology
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| ETEST LINEZOLID (K002139) | Ab Biodisk | 2000-11-08 |
| ETEST FOR QUINUPRISTIN/DALFOPRISTIN (K992993) | Ab Biodisk | 1999-11-16 |
Track LTX automatically
Every clearance here is in the API, with alerts when new ones post.