ClearanceBrief
510(k) K071826 ยท QEZ Aspiration Thrombectomy Catheter

THE RINSPIRATOR, MODELS FG09770, FG08776, FG08777, FG08910

ApplicantFox Hollow Technologies, Redwood City CA, US
DecisionSubstantially Equivalent, Nov 9, 2007
ReceivedJul 3, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K071826

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.