HIX
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Maxwell Spot, Ac-Powered
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 886.1435
- Medical specialty
- Ophthalmic
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| KARICKHOFF FLYING CORPUSCLE VIEWER (K831829) | Surgidev Corp. | 1983-10-19 |
| STERILE CAST PADDING (K801554) | Medi-Spec | 1980-08-04 |
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