ClearanceBrief
510(k) K813474 ยท KAM Cannula, Sinus

MAXILL-AIR SINUS VENTILATION TUBE

ApplicantXomed, Inc., Arnold MO, US
DecisionSubstantially Equivalent, Jan 12, 1982
ReceivedDec 1, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K813474

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.