ClearanceBrief
510(k) K942930 ยท FMI Needle, Hypodermic, Single Lumen

CAPCARD

ApplicantCapcard, Inc., Indianapolis IN, US
DecisionSubstantially Equivalent, Jul 10, 1995
ReceivedJun 22, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K942930

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.