ClearanceBrief
510(k) K905563 ยท KXO Monitor, Pressure, Intrauterine

INTRAN PLUS

ApplicantUtah Medical Products, Inc., Midvale UT, US
DecisionSubstantially Equivalent, Jun 19, 1991
ReceivedDec 12, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K905563

DateFirm and productCodeLinked 510(k)
Sep 11, 2008Utah Medical Products, Inc
Intran Plus, Disposable Intrauterine Pressure Catheter System, Part numbers IUP-400, IUP-400S, IUP-450, IUP-450S, IUP-500, IUP-550, IUP-600, IUP-600S, IUP-650, IUP-650S, IUP-700, IUP-750, Sterile, Sin
Terminated
HFNNone listed

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