PRIME ECG SYSTEM— 510(k) K012414

Substantially Equivalent

Meridian Medical Technologies, Inc.

FDA 510(k) clearance K012414 for PRIME ECG SYSTEM, Substantially Equivalent on 2002-03-06. Applicant: Meridian Medical Technologies, Inc..

Clearance details

Applicant: Meridian Medical Technologies, Inc.
Product code: Code DPS
Advisory panel: Cardiovascular
Date received: 2001-07-30
Decision date: 2002-03-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbia, MD, US

Download summary PDF View on FDA.gov ↗

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.