ClearanceBrief
510(k) K920626 ยท LOS

MODEL ELI 200 ELECTROCARDIOGRAPH

ApplicantMortara Instrument, Inc., Milwaukee WI, US
DecisionSubstantially Equivalent, Sep 4, 1992
ReceivedJan 29, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920626

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.