ClearanceBrief
510(k) K070539 ยท DPS Electrocardiograph

MORTARA ELI 10 ELECTROCARDIOGRAPH

ApplicantMortara Instrument, Inc., Milwaukee WI, US
DecisionSubstantially Equivalent, Mar 15, 2007
ReceivedFeb 26, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K070539

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.