ClearanceBrief
510(k) K882678 ยท ESD Hearing Aid, Air-Conduction, Prescription

ITE HEARING AID, SIEMENS MODEL 007, WITH TELOS

ApplicantSiemens Hearing Instruments, Inc., Piscataway NJ, US
DecisionSubstantially Equivalent, Sep 22, 1988
ReceivedJun 28, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882678

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.