ClearanceBrief
510(k) K920840 ยท MJV Device, Inflation, Middle Ear

OTOVENT

ApplicantAbigo Medical AB, Sweden, SE
DecisionSubstantially Equivalent, Oct 5, 1992
ReceivedFeb 24, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920840

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.