ClearanceBrief
510(k) K210065 ยท FMI Needle, Hypodermic, Single Lumen

Verifine Safety Type Insulin Pen Needle

ApplicantPromisemed Hangzhou Meditech Co., Ltd., Hangzhou City, CN
DecisionSubstantially Equivalent, Apr 22, 2021
ReceivedJan 11, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K210065

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.