CORDIS ENDOVASCULAR TEMPORARY OCCLUSION BALLOON CATHETER— 510(k) K984214

Substantially Equivalent

Cordis Neurovascular, Inc.

FDA 510(k) clearance K984214 for CORDIS ENDOVASCULAR TEMPORARY OCCLUSION BALLOON CATHETER, Substantially Equivalent on 1999-08-10. Applicant: Cordis Neurovascular, Inc..

Clearance details

Applicant: Cordis Neurovascular, Inc.
Product code: Code DXC
Advisory panel: Cardiovascular
Date received: 1998-11-24
Decision date: 1999-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami Lake, FL, US

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Adverse events under product code DXC

product code DXC

Death: 14
Injury: 442
Malfunction: 2,209
Other: 1
Total: 2,666

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.