ClearanceBrief
510(k) K880301 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function

3000 PHYSIOLOGICAL MONITOR

ApplicantDatascope Corp., Paramus NJ, US
DecisionSubstantially Equivalent, Aug 19, 1988
ReceivedJan 25, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880301

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.