510(k) K071737 ยท POV Semen Analysis Device
GENERAL SEMEN ANALYSIS KIT
| Applicant | Dyn-Bioshaf (2006) , Ltd., Rockville MD, US |
| Decision | Substantially Equivalent, Oct 25, 2007 |
| Received | Jun 26, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071737
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.