ClearanceBrief
510(k) K031652 ยท DQX Wire, Guide, Catheter

VASCUPUNCTURE PICC GUIDEWIRE

ApplicantNeometrics, Inc., Plymouth MN, US
DecisionSubstantially Equivalent, Sep 30, 2003
ReceivedMay 28, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K031652

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.