Clearance Summary
GMD UNIVERSAL CIRCUMCISION CLAMP, MODEL 200 received FDA 510(k) clearance under submission number K063429, sponsored by Generic Medical Device, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2007-01-17.
- Submission: K063429
- Applicant / Sponsor: Generic Medical Device, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.4530
- Decision date: 2007-01-17
Classification & Regulation
This clearance is catalogued under FDA product code HFX and 21 CFR 884.4530, within the Obstetrics/Gynecology review panel as a Class II device.