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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