ClearanceBrief
510(k) K771723 ยท KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube

HILL TUBE

ApplicantPhysio-Control Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 22, 1977
ReceivedSep 13, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K771723

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.