ClearanceBrief
510(k) K912418 ยท KAM Cannula, Sinus

SHIKANI MIDDLE MEATAL ANTROSTOMY VENT TUBE

ApplicantMicromedics, Inc., St. Paul MN, US
DecisionSubstantially Equivalent, Dec 20, 1991
ReceivedMay 31, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912418

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.