ClearanceBrief
510(k) K831319 ยท KLK Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia

PATIENT MONITOR #404

ApplicantAnalogic Corp., Walker MI, US
DecisionSubstantially Equivalent, Mar 22, 1984
ReceivedApr 22, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K831319

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.