ClearanceBrief
510(k) K896738 ยท DQA Oximeter

TYPE 9293 INTERFACE PULSEOX

ApplicantS & W Medico Teknik, Denmark, DK
DecisionSubstantially Equivalent, Aug 14, 1990
ReceivedNov 30, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896738

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.