ClearanceBrief
510(k) K760612 ยท DPS Electrocardiograph

SPACELABS SERIES 1000

ApplicantSpacelabs, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 21, 1976
ReceivedSep 10, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K760612

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.