510(k) K073039 ยท POV Semen Analysis Device
SPERMCHECK VASECTOMY
| Applicant | Princeton BioMeditech Corp., Monmouth Junction NJ, US |
| Decision | Substantially Equivalent, Jan 24, 2008 |
| Received | Oct 29, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073039
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.