ClearanceBrief
510(k) K901819 ยท DQA Oximeter

MODEL 78834C NEONATAL PULSE OXIMETER (SAO2)

ApplicantHewlett-Packard Co., Germany, DE
DecisionSubstantially Equivalent, Jul 18, 1990
ReceivedApr 23, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901819

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.