QUQ
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Knife, Intraocular Pressure Lowering
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4400
- Medical specialty
- General, Plastic Surgery
- FDA definition
- A knife intended for cutting of trabecular meshwork to reduce intraocular pressure in glaucoma
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| Kahook Dual Blade Glide (KDB Glide) (K220891) | New World Medical, Inc. | 2024-05-17 |
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Every clearance here is in the API, with alerts when new ones post.