FOLEY CATHETER— 510(k) K902710

Substantially Equivalent

Societa Gruppi Elastomeri S.A.

FDA 510(k) clearance K902710 for FOLEY CATHETER, Substantially Equivalent on 1990-11-21. Applicant: Societa Gruppi Elastomeri S.A..

Clearance details

Applicant: Societa Gruppi Elastomeri S.A.
Product code: Code EZL
Advisory panel: Gastroenterology, Urology
Date received: 1990-06-20
Decision date: 1990-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mendrisio, ES

Download summary PDF View on FDA.gov ↗

Adverse events under product code EZL

product code EZL

Death: 6
Injury: 796
Malfunction: 4,989
Other: 1
Total: 5,792

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.