ClearanceBrief
510(k) K935510 ยท DQA Oximeter

VX4 RECORDING PULSE OXIMETER

ApplicantVitalog Monitoring,Inc., Redwood CA, US
DecisionSubstantially Equivalent, Jul 1, 1994
ReceivedNov 16, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K935510

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.