ClearanceBrief
510(k) K171232 ยท KTI Bronchoscope Accessory

PeriView FLEX

ApplicantOlympus Surgical Technologies America, Southborough MA, US
DecisionSubstantially Equivalent, Sep 21, 2017
ReceivedApr 27, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K171232

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.