ClearanceBrief
510(k) K133635 ยท FMI Needle, Hypodermic, Single Lumen

EASYPOINT NEEDLE

ApplicantRetractable Technologies, Inc., Little Elm TX, US
DecisionSubstantially Equivalent, Jun 17, 2014
ReceivedNov 26, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K133635

DateFirm and productCodeLinked 510(k)
Mar 14, 2024Retractable Technologies, Inc.
EasyPoint Needle, 25G x 5/8", REF: 82091
Open, Classified
FMINone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.