ClearanceBrief
510(k) K932503 ยท ERA Otoscope

RI-MINI

ApplicantRudolf Riester GmbH & Co. KG, D-72417 Jungingen, DE
DecisionSubstantially Equivalent, Oct 8, 1993
ReceivedMay 21, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K932503

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.