ClearanceBrief
510(k) K934301 ยท HQZ Frame, Spectacle

SPECTACLE FRAMES

ApplicantGernot Lindner, Lunor-Vertrieb, Germany, DE
DecisionSubstantially Equivalent, Dec 8, 1993
ReceivedSep 2, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K934301

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.