ClearanceBrief
510(k) K242741 ยท FMI Needle, Hypodermic, Single Lumen

ACE Cannula

ApplicantAce Medical Industry Co., Ltd., Yangju-Si, KR
DecisionSubstantially Equivalent, Jan 8, 2025
ReceivedSep 11, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K242741

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.