ClearanceBrief
510(k) K933143 ยท LOS

MODEL ELI 300 ELECTROCARDIOGRAPH

ApplicantMortara Instrument, Inc., Milwaukee WI, US
DecisionSubstantially Equivalent, Apr 15, 1994
ReceivedJun 28, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K933143

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.