MDG
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- System, Intrafallopian Cannula
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 884.4530
- Medical specialty
- Obstetrics/Gynecology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| PBN FALLOPIAN TUBE CATHETER SYSTEM (K000620) | Medical Device Technologies, Inc. | 2000-10-30 |
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