ClearanceBrief
510(k) K053187 ยท DQX Wire, Guide, Catheter

AMPLATZER NOODLEWIRE GUIDEWIRE

ApplicantAga Medical Corp., Plymouth MN, US
DecisionSubstantially Equivalent, Apr 27, 2006
ReceivedNov 15, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K053187

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.