ClearanceBrief
510(k) K201699 ยท NLF Oximeter, Reprocessed

Medline ReNewal Reprocessed Nellcor OxiMax SpO2 Sensor

ApplicantSurgical Instrument and Savings Inc (Dba Medline Renewal), Redmond OR, US
DecisionSubstantially Equivalent, Jul 22, 2020
ReceivedJun 22, 2020
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K201699

No recall in the FDA data names this 510(k).

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