ClearanceBrief
510(k) K791364 ยท DPS Electrocardiograph

QUINTON MODEL 630 AND 636 ECG DATA CART

ApplicantQuinton, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 3, 1979
ReceivedJul 10, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K791364

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.