ClearanceBrief
510(k) K761098 ยท FMI Needle, Hypodermic, Single Lumen

FILTER DEVICES

ApplicantArrow Intl., Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 28, 1977
ReceivedNov 22, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K761098

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.