ClearanceBrief
510(k) K092306 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

SECURACATH UNIVERSAL

ApplicantInterrad Medical, Inc., Washington DC, US
DecisionSubstantially Equivalent, Jul 9, 2010
ReceivedJul 29, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K092306

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.