FDA Product Code
FDA Product Code HOO — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Ophthalmic
- 21 CFR Citation
- 886.1605
510(k) Clearances — 6 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K941723 | WELCH ALLYN GLAUCOMA DETECTOR | Welch Allyn, Inc. | 1994-06-06 | Traditional | PDF ↗ |
| K930448 | MARCO PROJECTION PERIMETER | Marco Ophthalmic, Inc. | 1993-06-21 | Traditional | PDF ↗ |
| K873912 | RICHMOND VISUAL FIELD SCREENER | Richmond Products, Inc. | 1987-11-02 | Traditional | PDF ↗ |
| K864467 | HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREEN | Keeler Instruments, Inc. | 1986-12-15 | Traditional | PDF ↗ |
| K860115 | DIGILAB CAMBRIDGE PERIMETER | Bio-Rad | 1986-02-27 | Traditional | PDF ↗ |
| K832800 | AUTOMATIC TANGENT SCREEN 50 | CooperVision, Inc. | 1983-09-29 | Traditional | PDF ↗ |
Product code HOO · Class I · Ophthalmic. Data: openFDA.