Product code MDG— Obstetrics/Gynecology
PBN FALLOPIAN TUBE CATHETER SYSTEM
- Classification name
- System, Intrafallopian Cannula
- Device class
- Class 2
- Regulation
- 21 CFR 884.4530
- Advisory panel
- Obstetrics/Gynecology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code MDG
FDA has cleared device under product code MDG, all in 2000, filed by 1 applicant company. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Top applicants under product code MDG
Recent clearances under product code MDG
Data sourced from openFDA. This site is unofficial and independent of the FDA.