MORTARA ELI 350 ELECTROCARDIOGRAPH— 510(k) K082946

Substantially Equivalent

Mortara Instrument, Inc.

FDA 510(k) clearance K082946 for MORTARA ELI 350 ELECTROCARDIOGRAPH, Substantially Equivalent on 2008-12-29. Applicant: Mortara Instrument, Inc..

Clearance details

Applicant: Mortara Instrument, Inc.
Product code: Code DPS
Advisory panel: Cardiovascular
Date received: 2008-10-02
Decision date: 2008-12-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milwaukee, WI, US

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Adverse events under product code DPS

product code DPS

Death: 7
Total: 7

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.