ClearanceBrief
510(k) K023251 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

PEDIATRIC ARTERIAL CANNULA

ApplicantPolystan A/S, Vaerlose, DK
DecisionSubstantially Equivalent, Dec 4, 2002
ReceivedSep 30, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K023251

DateFirm and productCodeLinked 510(k)
Aug 15, 2012Maquet Inc.
Maquet Getinge Group Pediatric Arterial Cannula Maquet Cardiopulmonary AG Kehler Strabe 31 76437 Rastatt Germany Phone +49 7222 932-0 Fax: +49 7222 932-1888 info.cp@maquet.com www.maquet.com Used to
Terminated
NCPNone listed

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