Clearance Summary
GENERAL SEMEN ANALYSIS KIT received FDA 510(k) clearance under submission number K071737, sponsored by Dyn-Bioshaf (2006) , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2007-10-25.
- Submission: K071737
- Applicant / Sponsor: Dyn-Bioshaf (2006) , Ltd.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.5220
- Decision date: 2007-10-25
Classification & Regulation
This clearance is catalogued under FDA product code POV and 21 CFR 864.5220, within the Hematology review panel as a Class II device.