HPO
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Magnet, Ac-Powered
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 886.4440
- Medical specialty
- Ophthalmic
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| INTRAOCULAR ELECTROMAGNET (K854870) | Mira, Inc. | 1986-02-19 |
| SCIENTRONICS 10K EYE MAGNET (K832950) | Scientific Manufacturer | 1983-10-19 |
| DORC INTRAOCULAR ELECTROMAGNET (K830336) | Jedmed Instrument Co. | 1983-03-09 |
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Every clearance here is in the API, with alerts when new ones post.