GENERAL SEMEN ANALYSIS KIT— 510(k) K071737
Substantially EquivalentDyn-Bioshaf (2006) , Ltd.
FDA 510(k) clearance K071737 for GENERAL SEMEN ANALYSIS KIT, Substantially Equivalent on 2007-10-25. Applicant: Dyn-Bioshaf (2006) , Ltd..
Clearance details
- Applicant
- Dyn-Bioshaf (2006) , Ltd.
- Product code
- Code POV
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rockville, MD, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.