EPCOM EMS-310 INTRAPARTUM MONITOR— 510(k) K831113

Substantially Equivalent

Epcom Medical Systems, Inc.

FDA 510(k) clearance K831113 for EPCOM EMS-310 INTRAPARTUM MONITOR, Substantially Equivalent on 1983-08-12. Applicant: Epcom Medical Systems, Inc..

Clearance details

Applicant: Epcom Medical Systems, Inc.
Product code: Code HGM
Advisory panel: Obstetrics/Gynecology
Date received: 1983-04-05
Decision date: 1983-08-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code HGM

product code HGM

Death: 35
Malfunction: 478
Total: 513

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.