ClearanceBrief
510(k) K101115 ยท DPS Electrocardiograph

ELI 150 ELECTROCARDIOGRAPH MODEL ELI 150

ApplicantMortara Instrument, Inc., Milwaukee WI, US
DecisionSubstantially Equivalent, Jun 18, 2010
ReceivedApr 21, 2010
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K101115

DateFirm and productCodeLinked 510(k)
Apr 29, 2020WELCH ALLYN, INC/MORTARA
Lead diagnostic electrocardiograph under the following device names: ELI 10, ELI 350, ELI 150c, ELI 250c, ELI 230, ELI 280, ELI 380, R-Scribe and Connex Cardio. Product Usage: A non-invasive prescr
Terminated
DPSNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.