INTIMAX THROMBECTOMY CATHETER— 510(k) K910372

Substantially Equivalent

Applied Vascular Devices, Inc.

FDA 510(k) clearance K910372 for INTIMAX THROMBECTOMY CATHETER, Substantially Equivalent on 1991-04-26. Applicant: Applied Vascular Devices, Inc..

Clearance details

Applicant: Applied Vascular Devices, Inc.
Product code: Code DXE
Advisory panel: Cardiovascular
Date received: 1991-01-29
Decision date: 1991-04-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Laguna Hills, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DXE

product code DXE

Death: 27
Injury: 258
Malfunction: 2,266
Total: 2,551

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.