ClearanceBrief
510(k) K203754 ยท MJV Device, Inflation, Middle Ear

Eustachi Ear Pressure Relief Device

ApplicantExercore, LLC, Shakopee MN, US
DecisionSubstantially Equivalent, Feb 19, 2021
ReceivedDec 23, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K203754

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.