THE BELLCO FISTULA NEEDLES— 510(k) K801632

Substantially Equivalent

Bellco Artifidial Organ Spec., Inc.

FDA 510(k) clearance K801632 for THE BELLCO FISTULA NEEDLES, Substantially Equivalent on 1980-08-04. Applicant: Bellco Artifidial Organ Spec., Inc..

Clearance details

Applicant: Bellco Artifidial Organ Spec., Inc.
Product code: Code FIE
Advisory panel: Gastroenterology, Urology
Date received: 1980-07-15
Decision date: 1980-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code FIE

product code FIE

Death: 2
Total: 2

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.