ClearanceBrief
510(k) K840334 ยท FMI Needle, Hypodermic, Single Lumen

CHEMONUCLEOLYSIS/DISCOGRAPHY TRAY

ApplicantApplied Medical Devices, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 13, 1984
ReceivedJan 25, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K840334

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.