ClearanceBrief
510(k) K100930 ยท DQX Wire, Guide, Catheter

PRIMEWIRE PRESTIAGE PRESSURE GUIDE WIRE, MODELS 8185, 8185J, 8300, 8300J

ApplicantVolcano Corporation, San Diego CA, US
DecisionSubstantially Equivalent, Apr 30, 2010
ReceivedApr 5, 2010
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K100930

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.