ANGIOJET ULTRA POWER PULSE KIT— 510(k) K130381

Substantially Equivalent

Medrad, Inc.

FDA 510(k) clearance K130381 for ANGIOJET ULTRA POWER PULSE KIT, Substantially Equivalent on 2013-07-29. Applicant: Medrad, Inc..

Clearance details

Applicant: Medrad, Inc.
Product code: Code QEW
Advisory panel: Cardiovascular
Date received: 2013-02-14
Decision date: 2013-07-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code QEW

product code QEW

Death: 126
Injury: 282
Malfunction: 820
Total: 1,228

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.