ClearanceBrief
510(k) K920980 ยท DQO Catheter, Intravascular, Diagnostic

USCI LINX EZ GUIDE WIRE EXTENSION W/PRO/PEL COAT

ApplicantC.R. Bard, Inc., Billerica MA, US
DecisionSubstantially Equivalent, Aug 24, 1992
ReceivedMar 2, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920980

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.