FDA Product Code
FDA Product Code HOW — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Ophthalmic
- 21 CFR Citation
- 886.1200
510(k) Clearances — 1 record
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K822917 | MODEL 5400 OPTOKINETIC STIMULATOR | Life-Tech Intl., Inc. | 1982-11-01 | Traditional | PDF ↗ |
Product code HOW · Class I · Ophthalmic. Data: openFDA.