ClearanceBrief
510(k) K852959 ยท KLK Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia

PO-510 TCPO2 MONITOR

ApplicantSumitomo Electric Industries, Inc., Osaka, 554 Japan, JP
DecisionSubstantially Equivalent, Nov 29, 1985
ReceivedJul 12, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K852959

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.