510(k) K161785 ยท KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube
THD ANOPRESS
| Applicant | Thd Spa, Correggio, IT |
| Decision | Substantially Equivalent, Mar 14, 2017 |
| Received | Jun 29, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161785
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.