ClearanceBrief
510(k) K951828 ยท ESD Hearing Aid, Air-Conduction, Prescription

FULL DYNAMIC RANGE COMPRESSION BEHIND THE EAR HEARING INSTRUMENT

ApplicantSiemens Hearing Instruments, Inc., Piscataway NJ, US
DecisionSubstantially Equivalent, Jun 30, 1995
ReceivedApr 20, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K951828

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.