ClearanceBrief
510(k) K874430 ยท FMI Needle, Hypodermic, Single Lumen

NEEDLE CONTAINER

ApplicantAmerican Medical Technology, Inc., Brooklyn CT, US
DecisionSubstantially Equivalent, Jan 4, 1988
ReceivedOct 28, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K874430

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.