510(k) K252228 ยท POV Semen Analysis Device
Seaman Pro/Seaman
| Applicant | Checkcells, Inc., Santa Monica CA, US |
| Decision | Substantially Equivalent, Apr 9, 2026 |
| Received | Jul 16, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252228
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.