510(k) K100341 ยท POV Semen Analysis Device
SPERMCHECK FERTILITY
| Applicant | Princeton BioMeditech Corp., Monmouth Junction NJ, US |
| Decision | Substantially Equivalent, May 4, 2010 |
| Received | Feb 5, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100341
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.