ClearanceBrief
510(k) K791156 ยท FMI Needle, Hypodermic, Single Lumen

AMIPAQUE MYELOGRAM TRAY

ApplicantPharmaseal Div., Baxter Healthcare Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 30, 1979
ReceivedJun 21, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K791156

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.