ClearanceBrief
510(k) K935505 ยท FMI Needle, Hypodermic, Single Lumen

WINGED COLLECTION SET W/MULTI-SAMPLE LUER ADAPTER

ApplicantKawasumi Laboratories Co., Ltd., Tokyo, JP
DecisionSubstantially Equivalent, Feb 3, 1994
ReceivedNov 16, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K935505

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.