ClearanceBrief
510(k) K063217 ยท DTK Filter, Intravascular, Cardiovascular

VENATECH LP BRACHIAL INTRODUCER SYSTEM (ANTECUBITAL)

ApplicantB.Braun Medical, Inc., Bethlehem PA, US
DecisionSubstantially Equivalent, Jan 12, 2007
ReceivedOct 24, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K063217

DateFirm and productCodeLinked 510(k)
Nov 24, 2007B. Braun Interventional Systems
Vena Tech LP Vena Cava Filter System, Item No/REF. 05010024, Model No: 40DLP, B Braun. Manufacturer: B. Braun Medical 204, avenue du Marechal Juin BP 331 92107 Boulogne Cedex , France. (The VenaTech L
Terminated
DTKNone listed

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