ClearanceBrief
510(k) K944284 ยท DQO Catheter, Intravascular, Diagnostic

CONTROL

ApplicantDaig Corp., Minnetonka MN, US
DecisionSubstantially Equivalent, Mar 3, 1995
ReceivedSep 2, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K944284

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.