ClearanceBrief
510(k) K072059 ยท FMI Needle, Hypodermic, Single Lumen

GRIPPER MICRO NEEDLE

ApplicantSmiths Medical MD, Inc., St. Paul MN, US
DecisionSubstantially Equivalent, Nov 1, 2007
ReceivedJul 26, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K072059

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.