ClearanceBrief
510(k) K003642 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

PLACEMENT-PLUS

ApplicantCatheter Innovations, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Dec 20, 2000
ReceivedNov 27, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K003642

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.