510(k) K231702 · FAJ Cystoscope And Accessories, Flexible/Rigid
WiScope® Digital Cystoscope System, WiScope® Single-Use Digital Flexible Cystoscope, WiScope® Medical Tablet
| Applicant | OTU Medical, Inc., Union City CA, US |
| Decision | Substantially Equivalent, Sep 29, 2023 |
| Received | Jun 12, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231702
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.