NCR
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Apparatus, Cutting, Radiofrequency, Electrosurgical, Battery-Powered
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 886.4100
- 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 |
|---|---|---|
| FUGO BLADE FOR PERIPHERAL IRIDOTOMY, MODEL M300 (K050933) | Medisurg , Ltd. | 2005-12-09 |
| THE FUGO BLADE FOR GLAUCOMA (K041019) | Medisurg , Ltd. | 2004-10-08 |
| THE FUGO BLADE (K001498) | Medisurg , Ltd. | 2000-08-10 |
Track NCR automatically
Every clearance here is in the API, with alerts when new ones post.