ClearanceBrief
510(k) K020285 ยท GWM Device, Monitoring, Intracranial Pressure

CMA CEREBRAL TISSUE MONITORING SYSTEM

ApplicantCma Microdialysis AB, North Attleboro MA, US
DecisionSubstantially Equivalent, Oct 23, 2002
ReceivedJan 28, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K020285

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.