ClearanceBrief
510(k) K891248 ยท ESD Hearing Aid, Air-Conduction, Prescription

BEHIND-THE-EAR HEARING AID MODEL 304 PP-AGC-I

ApplicantSiemens Hearing Instruments, Inc., Piscataway NJ, US
DecisionSubstantially Equivalent, Mar 29, 1989
ReceivedMar 8, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K891248

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.