ClearanceBrief
510(k) K980227 ยท FMI Needle, Hypodermic, Single Lumen

MANAN GALACTOGRAPHY KIT

ApplicantMedical Device Technologies, Inc., Gainsville FL, US
DecisionSubstantially Equivalent, Apr 23, 1998
ReceivedJan 22, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980227

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.