HIW
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Anomaloscope
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 886.1070
- Medical specialty
- Ophthalmic
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| KAMPPETER ANOMALOSCOPE (K930575) | Bova Intl. | 1994-02-25 |
| ANOMALOSCOPE QUADRANT TEST-6 (K913962) | Lkc Technologies, Inc. | 1991-10-23 |
| GUNKEL CHROMAGRAPH COLOR VISION TESTER (K860174) | Chromagraphics, Inc. | 1986-04-04 |
Track HIW automatically
Every clearance here is in the API, with alerts when new ones post.