ClearanceBrief
510(k) K862621 ยท ERA Otoscope

I22 INITIALES

ApplicantOticon Corp., Somerset NJ, US
DecisionSubstantially Equivalent, Aug 1, 1986
ReceivedJul 10, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862621

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.