DIAGNOSTIC INTRASCULAR CATHETER— 510(k) K903848

Substantially Equivalent

Applied Vascular Devices, Inc.

FDA 510(k) clearance K903848 for DIAGNOSTIC INTRASCULAR CATHETER, Substantially Equivalent on 1991-03-25. Applicant: Applied Vascular Devices, Inc..

Clearance details

Applicant: Applied Vascular Devices, Inc.
Product code: Code DQO
Advisory panel: Cardiovascular
Date received: 1990-08-21
Decision date: 1991-03-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Laguna Hills, CA, US

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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.