ClearanceBrief
510(k) K901125 ยท KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube

PROVOCATIVE SENSITIVITY BALLOON

ApplicantWilson-Cook Medical, Inc., Winston-Salem NC, US
DecisionSubstantially Equivalent, Jan 25, 1991
ReceivedMar 12, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901125

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.