ClearanceBrief
510(k) K970269 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

CLINICATH IR PERIPHERALLY INSERTED CATHETER

ApplicantSims Deltec, Inc., St. Paul MN, US
DecisionSubstantially Equivalent, Jun 26, 1997
ReceivedJan 23, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970269

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.