Q4000 AND Q3040 ELECTROCARDIOGRAPH MONITOR— 510(k) K863159

Substantially Equivalent

Quinton, Inc.

FDA 510(k) clearance K863159 for Q4000 AND Q3040 ELECTROCARDIOGRAPH MONITOR, Substantially Equivalent on 1986-10-06. Applicant: Quinton, Inc..

Clearance details

Applicant: Quinton, Inc.
Product code: Code DSI
Advisory panel: Cardiovascular
Date received: 1986-08-18
Decision date: 1986-10-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, US

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Adverse events under product code DSI

product code DSI

Death: 170
Injury: 729
Malfunction: 10,680
Total: 11,579

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.