ClearanceBrief
510(k) K900700 ยท DPS Electrocardiograph

SMU 611 UNIVERSALMONITOR

ApplicantPpg Industries, Inc., Lenexa KS, US
DecisionSubstantially Equivalent, Apr 3, 1990
ReceivedFeb 12, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900700

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.