ClearanceBrief
510(k) K880346 ยท HMX Cannula, Ophthalmic

CANNULAS

ApplicantMyocure, Inc., Glendale CA, US
DecisionSubstantially Equivalent, May 3, 1988
ReceivedJan 26, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880346

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.