ClearanceBrief
510(k) K032733 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

PM-8000 PATIENT MONITOR, MODEL 8000

ApplicantShenzhen Mindray Bio-Medical Electronics Co., Ltd., Great Neck NY, US
DecisionSubstantially Equivalent, Mar 3, 2004
ReceivedSep 4, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K032733

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.