ClearanceBrief
510(k) K830573 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

PRE VUE

ApplicantTaut, Inc., Walker MI, US
DecisionSubstantially Equivalent, Mar 29, 1983
ReceivedFeb 23, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830573

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.