ClearanceBrief
510(k) K101280 ยท NLF Oximeter, Reprocessed

MIDWESTERN REPROCESSING CENTER REPROCESSED PULSE OXIMETER PROBE

ApplicantMidwest Reprocessing Center, LLC, Birmingham AL, US
DecisionSubstantially Equivalent, Oct 7, 2010
ReceivedMay 6, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K101280

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.