FDA Product Code
FDA Product Code MYD — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Ophthalmic
- 21 CFR Citation
- 886.4370
510(k) Clearances — 1 record
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K991124 | VISIJET HYDROKERATOME, MODEL 50 | Visijet, Inc. | 2000-10-20 | Traditional | PDF ↗ |
Product code MYD · Class I · Ophthalmic. Data: openFDA.