ClearanceBrief
510(k) K120420 ยท FMI Needle, Hypodermic, Single Lumen

STERILE BLUNT FOR SINGLE USE

ApplicantShanghai Double Dove Industrial Co., Ltd., Shanghai, CN
DecisionSubstantially Equivalent, Oct 18, 2012
ReceivedFeb 10, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K120420

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.