ClearanceBrief
510(k) K042316 ยท NLF Oximeter, Reprocessed

VANGUARD REPROCESSED PULSE OXIMETER SENSORS

ApplicantVanguard Medical Concepts, Inc., Lakeland FL, US
DecisionSubstantially Equivalent, Jan 6, 2005
ReceivedAug 26, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K042316

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.