ClearanceBrief
510(k) K062677 ยท DPS Electrocardiograph

ELI 350 ELECTROCARDIOGRAPH

ApplicantMortara Instrument, Inc., Milwaukee WI, US
DecisionSubstantially Equivalent, Nov 15, 2006
ReceivedSep 8, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K062677

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.