ClearanceBrief
510(k) K854742 ยท ESD Hearing Aid, Air-Conduction, Prescription

OTICON, CITEC CUSTOM MADE HEARING AID CANAL TYPE

ApplicantOticon Corp., Somerset NJ, US
DecisionSubstantially Equivalent, Feb 20, 1986
ReceivedNov 25, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854742

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.