ClearanceBrief
510(k) K961088 ยท FMI Needle, Hypodermic, Single Lumen

NON-CORING NEEDLE

ApplicantArrow Intl., Inc., Walpole MA, US
DecisionSubstantially Equivalent, Jul 2, 1996
ReceivedMar 19, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961088

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.