MODIFICATION TO BARD AQUAGUIDE URETERAL CONDUIT— 510(k) K033778

Substantially Equivalent

C.R. Bard, Inc.

FDA 510(k) clearance K033778 for MODIFICATION TO BARD AQUAGUIDE URETERAL CONDUIT, Substantially Equivalent on 2003-12-30. Applicant: C.R. Bard, Inc..

Clearance details

Applicant: C.R. Bard, Inc.
Product code: Code FED
Advisory panel: Gastroenterology, Urology
Date received: 2003-12-04
Decision date: 2003-12-30
Decision: Substantially Equivalent
Clearance type: Special
Location: Covington, GA, US

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Adverse events under product code FED

product code FED

Death: 10
Total: 10

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.