MUS
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Fluidic, Phacoemulsification/Phacofragmentation
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 886.4670
- Medical specialty
- Ophthalmic
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| CATARACT LIQUEFRACTURE DEVICE (K980292) | Alcon Laboratories | 1998-05-19 |
Track MUS automatically
Every clearance here is in the API, with alerts when new ones post.