ClearanceBrief
510(k) K812167 ยท KLK Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia

MODEL 78850 OXYGEN MONITOR

ApplicantHewlett-Packard Co., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 31, 1981
ReceivedJul 30, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812167

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.