ClearanceBrief
510(k) K874024 ยท FMI Needle, Hypodermic, Single Lumen

ACU-MICRO-NEEDLE

ApplicantAcuderm, Inc., Ft. Lauderdale FL, US
DecisionSubstantially Equivalent, Nov 23, 1987
ReceivedOct 2, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K874024

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.