ClearanceBrief
510(k) K020252 ยท FMF Syringe, Piston

SMARTJET GRAFTING LIQUID APPLICATOR, MODELS SK/S & LK/2

ApplicantHarvest Technologies, Corp., Plymouth MA, US
DecisionSubstantially Equivalent, Apr 5, 2002
ReceivedJan 24, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K020252

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.