ClearanceBrief
510(k) K820172 ยท ESD Hearing Aid, Air-Conduction, Prescription

PHONIC EAR MODEL PE 810S

ApplicantPhonic Ear, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 24, 1982
ReceivedJan 21, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820172

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.