HOO
6 FDA 510(k) clearances · Product code
45 daysmedian time to decision
146 days90th percentile
6clearances measured
FDA profile
- Official device name
- Perimeter, Ac-Powered
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 886.1605
- Medical specialty
- Ophthalmic
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| WELCH ALLYN GLAUCOMA DETECTOR (K941723) | Welch Allyn, Inc. | 1994-06-06 |
| MARCO PROJECTION PERIMETER (K930448) | Marco Ophthalmic, Inc. | 1993-06-21 |
| RICHMOND VISUAL FIELD SCREENER (K873912) | Richmond Products, Inc. | 1987-11-02 |
| HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREEN (K864467) | Keeler Instruments, Inc. | 1986-12-15 |
| DIGILAB CAMBRIDGE PERIMETER (K860115) | Bio-Rad | 1986-02-27 |
| AUTOMATIC TANGENT SCREEN 50 (K832800) | CooperVision, Inc. | 1983-09-29 |
Track HOO automatically
Every clearance here is in the API, with alerts when new ones post.