ClearanceBrief
510(k) K093409 ยท HRX Arthroscope

POWERPUMP ARTHROSCOPY SYSTEM

ApplicantMedical Vision AB, Ne MN, US
DecisionSubstantially Equivalent, Feb 24, 2010
ReceivedNov 2, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K093409

DateFirm and productCodeLinked 510(k)
May 10, 2016Medical Vision Ab
Double Pump RF Patient Cassette; Product Number: 72204055. Intended to provide fluid distension and irrigation and fluid suction during diagnostic and operative arthroscopic procedures.
Terminated
HRXNone listed

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