510(k) K180135 ยท KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube
THD Anopress with THD SensyProbe
| Applicant | Thd Spa, Correggio, IT |
| Decision | Substantially Equivalent, Mar 8, 2018 |
| Received | Jan 17, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180135
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.