ClearanceBrief
510(k) K082946 ยท DPS Electrocardiograph

MORTARA ELI 350 ELECTROCARDIOGRAPH

ApplicantMortara Instrument, Inc., Milwaukee WI, US
DecisionSubstantially Equivalent, Dec 29, 2008
ReceivedOct 2, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K082946

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.