ClearanceBrief
510(k) K830413 ยท HQZ Frame, Spectacle

HANDPIECE SYSTEM I/A

ApplicantUxtra Corp., Walker MI, US
DecisionSubstantially Equivalent, Apr 5, 1983
ReceivedFeb 8, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830413

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.