ClearanceBrief
510(k) K782169 ยท HMX Cannula, Ophthalmic

NEEDLES, CANNULAS, CYSTOTOMES

ApplicantVisitec Co., Walker MI, US
DecisionSubstantially Equivalent, Feb 13, 1979
ReceivedDec 29, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K782169

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.