ClearanceBrief
510(k) K992631 ยท DQO Catheter, Intravascular, Diagnostic

ACUNAV DIAGNOSTIC ULTRASOUND CATHETER

ApplicantAcuson Corp., Washington DC, US
DecisionSubstantially Equivalent, Dec 15, 1999
ReceivedAug 6, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K992631

DateFirm and productCodeLinked 510(k)
Mar 23, 2011Siemens Medical Solutions USA, Inc.
Siemens Medical Solutions USA, Inc., ACUSON AcuNav ultrasound catheters when using SwiftLink catheter connectors; Model Number: 10348560.
Terminated
DQONone listed

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