ClearanceBrief
510(k) K182868 ยท MUD Oximeter, Tissue Saturation

INVOS PM7100 Patient Monitor, INVOS Adult rSO2 Sensor

ApplicantCovidien, LLC, Boulder CO, US
DecisionSubstantially Equivalent, Jan 8, 2019
ReceivedOct 12, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K182868

DateFirm and productCodeLinked 510(k)
Apr 30, 2024Covidien
Medtronic Invos, Reusable Sensor Cable for PM7100, REF: PMAC71RSC
Open, Classified
MUDNone listed

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