ClearanceBrief
510(k) K923653 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

NEEDLELESS INJECTION CANNULA

ApplicantArrow Intl., Inc., Reading PA, US
DecisionSubstantially Equivalent, May 13, 1993
ReceivedJul 21, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923653

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.