ClearanceBrief
510(k) K952222 ยท DQA Oximeter

NELLCOR N-20PA PORTABLE PULSE OXIMETER

ApplicantNellcor, Inc., Pleasanton CA, US
DecisionSubstantially Equivalent, Aug 15, 1995
ReceivedMay 12, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K952222

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.