510(k) K234107 · KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube
Solar Anorectal Manometry Catheter (Model Number: K1210AC-L-2212)
| Applicant | Laborie Medical Technologies, Corp., Portsmouth NH, US |
| Decision | Substantially Equivalent, Apr 23, 2024 |
| Received | Dec 26, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K234107
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.