510(k) K242304 ยท KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube
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| Applicant | Neuraxis, Inc., Carmel IN, US |
| Decision | Substantially Equivalent, Dec 6, 2024 |
| Received | Aug 5, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242304
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.