IWW
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Shield, Vial
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 892.6500
- Medical specialty
- Radiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| ALL-VUE & GAMMA-VUE VIAL SHIELDS (K934548) | Victoreen, Inc. | 1993-11-12 |
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Every clearance here is in the API, with alerts when new ones post.