ClearanceBrief
510(k) K912199 ยท DQY Catheter, Percutaneous

SOFTTOUCH(R) GUIDING CATHETER

ApplicantMallinckrodt Medical, St Louis MO, US
DecisionSubstantially Equivalent, Jul 30, 1991
ReceivedMay 17, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912199

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.