ClearanceBrief
510(k) K013478 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive

DYNAPULSE 5200A PATHWAY BLOOD PRESSURE MONITORING SYSTEM

ApplicantPulse Metric, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Jan 10, 2002
ReceivedOct 19, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K013478

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.