ClearanceBrief
510(k) K141634 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

NAUTILUS DELTA

ApplicantRomedex International Srl, San Francisco CA, US
DecisionSubstantially Equivalent, Jan 27, 2015
ReceivedJun 18, 2014
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K141634

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.