ClearanceBrief
510(k) K930203 ยท EWD Protector, Hearing (Insert)

MODEL 322 CLINICAL AUDIOMETER

ApplicantVirtual Corp., Portland OR, US
DecisionSubstantially Equivalent, Jul 8, 1993
ReceivedJan 14, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K930203

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.