ClearanceBrief
510(k) K060756 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

MEDLOG, MODEL 1-0-10

ApplicantBmc Gesellschaft Fur Medizintechnik Mbh, Hamburg, DE
DecisionSubstantially Equivalent, Oct 30, 2006
ReceivedMar 21, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K060756

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.