ClearanceBrief
510(k) K935095 ยท ESD Hearing Aid, Air-Conduction, Prescription

8260 SERIES 3M PROGRAMMABLE HEARING INSTRUMENTS

Applicant3M Company, St. Paul MN, US
DecisionSubstantially Equivalent, Dec 15, 1993
ReceivedOct 25, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K935095

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.