ClearanceBrief
510(k) K895770 ยท FPA Set, Administration, Intravascular

EXEL HUBER INFUSION SET

ApplicantExel Intl., Culver City CA, US
DecisionSubstantially Equivalent, Jul 19, 1990
ReceivedSep 26, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895770

DateFirm and productCodeLinked 510(k)
Jan 22, 2010Exelint International Co.
Exel Huber Infusion Set (Catalog Numbers 26940R, 26941R, 26944R, 26945R, 26946R, 26948R, 26949R, 26950R, 27940R, 27941R, 27944R, 27945R, 27946R, 27948R, 27949R, 27950R, 26954R, 26955R, 26958R, 26959R,
Terminated
FPANone listed

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