ClearanceBrief
510(k) K922553 ยท KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube

CLA-COMPUTERIZED LARYNGEAL ANALYZER

ApplicantH.I.L. Research, Ltd., Chico CA, US
DecisionSubstantially Equivalent, Aug 23, 1994
ReceivedMay 29, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922553

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.