ClearanceBrief
510(k) K030467 ยท FPA Set, Administration, Intravascular

GRAVITECH TM FLOW CONTROLLER PRIMARY SET/GRAVITECH FLOW CONTROLLER EXTENSION SET

ApplicantIv Medical, Inc., Carlsbad CA, US
DecisionSubstantially Equivalent, Mar 14, 2003
ReceivedFeb 12, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030467

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.