METRICATH SYSTEM— 510(k) K042685

Substantially Equivalent

Angiometrx, Inc.

FDA 510(k) clearance K042685 for METRICATH SYSTEM, Substantially Equivalent on 2004-11-18. Applicant: Angiometrx, Inc..

Clearance details

Applicant: Angiometrx, Inc.
Product code: Code DQO
Advisory panel: Cardiovascular
Date received: 2004-09-29
Decision date: 2004-11-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Vancouver, Bc, CA

Download summary PDF View on FDA.gov ↗

Adverse events under product code DQO

product code DQO

Death: 35
Injury: 993
Malfunction: 1,772
Other: 5
Total: 2,805

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.