ClearanceBrief
510(k) K883297 ยท DQA Oximeter

HEWLETT-PACKARD MODLES 78354A/78352 PULSE OXIMETER

ApplicantHewlett-Packard Co., Waltham MA, US
DecisionSubstantially Equivalent, Oct 6, 1988
ReceivedAug 4, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883297

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.