KYH
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Endoscope, Ophthalmic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.1500
- Medical specialty
- Gastroenterology, Urology
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| GM OPTI*CAM CAMERA WITH FIBER OPTIC LIGHT (K941660) | Gm Engineering, Inc. | 1994-05-24 |
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Every clearance here is in the API, with alerts when new ones post.