FDA Product Code
FDA Product Code HOK — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Ophthalmic
- 21 CFR Citation
- 886.1810
510(k) Clearances — 1 record
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K914896 | FRIEDMANN ANALYSER 3 | Clement Clarke, Inc. | 1992-01-23 | Traditional | PDF ↗ |
Product code HOK · Class I · Ophthalmic. Data: openFDA.