CORDIS VENTRICULAR ANTECHAMBER (VA)— 510(k) K955832

Substantially Equivalent

Cordis Corp.

FDA 510(k) clearance K955832 for CORDIS VENTRICULAR ANTECHAMBER (VA), Substantially Equivalent on 1996-03-25. Applicant: Cordis Corp..

Clearance details

Applicant: Cordis Corp.
Product code: Code JXG
Advisory panel: Neurology
Date received: 1995-12-26
Decision date: 1996-03-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami Lakes, FL, US

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Adverse events under product code JXG

product code JXG

Death: 76
Injury: 5,632
Malfunction: 2,230
Other: 4
Total: 7,942

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.