MOK
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Vaginoscope And Accessories
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 884.1630
- Medical specialty
- Obstetrics/Gynecology
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| GelPOINT V-Path Vaginal Access System (K220969) | Applied Medical Resources Corporation | 2022-09-16 |
| KARL STORZ INFANT, BALLOON VAGINOSCOPE, VAGINOSCOPE SHEATH, FIBER OPTIC LIGHT CARRIERS, ADJUSTABLE MAGNIFIERS (K950639) | KARL STORZ Endoscopy-America, Inc. | 1995-06-19 |
Track MOK automatically
Every clearance here is in the API, with alerts when new ones post.