ClearanceBrief
510(k) K834091 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

SILCATH

ApplicantHdc Corp., Walker MI, US
DecisionSubstantially Equivalent, Mar 6, 1984
ReceivedNov 28, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K834091

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.