ClearanceBrief
510(k) K881612 ยท ESD Hearing Aid, Air-Conduction, Prescription

DAHLBERG MODEL XJ 8080 BODY-WORN HEARING AID

ApplicantDahlberg Electronics, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Jun 1, 1988
ReceivedApr 12, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K881612

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.