ClearanceBrief
510(k) K081210 ยท FPA Set, Administration, Intravascular

NIPRO SAFETOUCH HUBER INFUSTION SET

ApplicantNipro Medical Corp., Miami FL, US
DecisionSubstantially Equivalent, Oct 21, 2008
ReceivedApr 29, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K081210

DateFirm and productCodeLinked 510(k)
Jan 22, 2010Exelint International Co.
Exel Safety Huber Infusion Sets (20G and 22G sizes with Catalog Numbers 37854S, 37855S. 37858S).
Terminated
FPANone listed

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