ClearanceBrief
510(k) K791963 ยท DYB Introducer, Catheter

USCI MULLINS TRANSSEPTAL CATHETER INTRO.

ApplicantC.R. Bard, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 13, 1979
ReceivedOct 1, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K791963

DateFirm and productCodeLinked 510(k)
Aug 5, 2013Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic Mullins Transseptal Adult 7F, REF 008551. Intended for the introduction of cardiovascular catheters into the left side of the heart.
Terminated
DYBNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.