ClearanceBrief
510(k) K030780 ยท CBK Ventilator, Continuous, Facility Use

NEWPORT E500 WAVE VENTILATOR

ApplicantNewport Medical Instruments, Inc., Costa Mesa CA, US
DecisionSubstantially Equivalent, Jan 23, 2004
ReceivedMar 11, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030780

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.