ClearanceBrief
510(k) K945323 ยท HQZ Frame, Spectacle

SPECTACLE FRAME

ApplicantM.Y. Vision Corp., Paramus NJ, US
DecisionSubstantially Equivalent, Nov 22, 1994
ReceivedNov 1, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K945323

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.