ClearanceBrief
510(k) K884065 ยท DQO Catheter, Intravascular, Diagnostic

CATH LAB MONITORING CATHETER

ApplicantC.R. Bard, Inc., Tewksbury MA, US
DecisionSubstantially Equivalent, Jan 12, 1989
ReceivedSep 26, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884065

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.