MYD
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Keratome, Water Jet
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 886.4370
- Medical specialty
- Ophthalmic
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| VISIJET HYDROKERATOME, MODEL 50 (K991124) | Visijet, Inc. | 2000-10-20 |
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Every clearance here is in the API, with alerts when new ones post.