ClearanceBrief
510(k) K052795 ยท HGM System, Monitoring, Perinatal

PHILIPS AVALON FETAL MONITOR, MODELS FM20 AND FM30

ApplicantPhilips Medizin Systeme Boeblingen GmbH, Boeblingen, Baden-Wuerttemberg, DE
DecisionSubstantially Equivalent, Dec 30, 2005
ReceivedOct 3, 2005
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K052795

DateFirm and productCodeLinked 510(k)
Dec 17, 2009Philips Healthcare Inc.
Philips Avalon Fetal Monitor FM 30 Catalog Number: M2703A.
Terminated
HGMNone listed

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