ClearanceBrief
510(k) K875057 ยท DPS Electrocardiograph

FUKUDA MODEL DS-503 DYNASCOPE PATIENT MONITOR

ApplicantFukuda Denshi USA, Inc., Kirkland WA, US
DecisionSubstantially Equivalent, Mar 22, 1988
ReceivedDec 9, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K875057

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.