IZS
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Aperture, Radiographic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 892.1610
- Medical specialty
- Radiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| APERTURE (K895084) | Custom Medical Products, Ltd. | 1989-10-27 |
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