ClearanceBrief
510(k) K060230 ยท HGM System, Monitoring, Perinatal

DOPPLEX CENTRALE

ApplicantHuntleigh Healthcare , Ltd., Cardiff, GB
DecisionSubstantially Equivalent, Mar 23, 2006
ReceivedJan 30, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K060230

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.