ClearanceBrief
510(k) K860744 ยท HMX Cannula, Ophthalmic

OPTHALMIC SURGICAL INSTRUMENTS

ApplicantTridak Division of Indicon, Inc., Pearl River NY, US
DecisionSubstantially Equivalent, Mar 31, 1986
ReceivedFeb 27, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860744

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.