ClearanceBrief
510(k) K895769 ยท FMI Needle, Hypodermic, Single Lumen

EXEL HUBER NEEDLE

ApplicantExel Intl., Culver City CA, US
DecisionSubstantially Equivalent, Feb 16, 1990
ReceivedSep 26, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895769

DateFirm and productCodeLinked 510(k)
Jan 22, 2010Exelint International Co.
Exel Huber Needles (Right angle and Straight Models with Catalog Numbers: 26901CE, 26902CE, 26903CE, 26904CE, 26905CE, 26906CE, 26907CE, 26908CE, 26909CE, 26910CE, 26911CE, 26921CE, 26922CE, 26923CE,
Terminated
FMINone listed

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