ClearanceBrief
510(k) K901774 ยท DQA Oximeter

HORIZON 2000 PULSE OXIMETRY (SAO2) MONITOR CAPABIL

ApplicantMennen Medical, Inc., Clarence NY, US
DecisionSubstantially Equivalent, May 22, 1990
ReceivedApr 19, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901774

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.