Product code FHG— Obstetrics/Gynecology
CIRCUMCISION KIT
- Classification name
- Bell, Circumcision
- Device class
- Class 2
- Regulation
- 21 CFR 884.4530
- Advisory panel
- Obstetrics/Gynecology
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code FHG
FDA has cleared devices under product code FHG between 1977 and 1991, filed by 2 applicant companies. 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.
Clearances per year
- 1991
- 1977
Top applicants under product code FHG
Recent clearances under product code FHG
Data sourced from openFDA. This site is unofficial and independent of the FDA.