LWI
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Ultrasound, Sinus
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 892.1560
- Medical specialty
- Radiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| SINUSCAN 102/SINUSPRINT (K960421) | Ferguson Medical | 1997-04-16 |
| ULTRAMAX/MODEL NUMBER A1 (K960044) | Entlab OY | 1996-08-02 |
| CPR GENERAL SURGERY TRAY (K960241) | Custom Pack Reliability | 1996-03-22 |
| ENTERSCAN (K874081) | Pie Data Medical BV | 1987-12-31 |
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