MDG
2000-10-30
System, Intrafallopian Cannula
FDA product code MDG · 1 cleared devices
Class 2
Obstetrics/Gynecology
- Regulation
- 21 CFR 884.4530
- Review panel
- OB
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 2000-10-30 – 2000-10-30
No matching devices.
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