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FDA 510(k) Applications Submitted by MORTARA INSTRUMENT, INC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K142105
08/01/2014
ELI 380 ELECTROCARDIOGRAPH
MORTARA INSTRUMENT, INC
K120865
03/22/2012
RSCRIBE ELECTROCARDIOGRAPH
MORTARA INSTRUMENT, INC
K101115
04/21/2010
ELI 150 ELECTROCARDIOGRAPH MODEL ELI 150
MORTARA INSTRUMENT, INC
K152626
09/15/2015
H3+ Holter Recorder
MORTARA INSTRUMENT, INC
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