ClearanceBrief
510(k) K982018 ยท FMF Syringe, Piston

LIGHT SABER ASPIRATION NEEDLE

ApplicantMinrad, Inc., Orchard Park NY, US
DecisionSubstantially Equivalent, Aug 7, 1998
ReceivedJun 8, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K982018

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.