ClearanceBrief
510(k) K934685 ยท DQY Catheter, Percutaneous

SOFTTOUCH GUIDE CATHETER

ApplicantMallinckrodt Medical, St Louis MO, US
DecisionSubstantially Equivalent, Apr 7, 1994
ReceivedSep 30, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K934685

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.