510(k) K242666 ยท KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube
Fecobionics Anorectal System
| Applicant | Gi Bionics, LLC, San Diego CA, US |
| Decision | Substantially Equivalent, Feb 12, 2025 |
| Received | Sep 5, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242666
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.