FOLEY CATHETER— 510(k) K902710

Name: FDA 510(k) clearance K902710
Creator: U.S. Food and Drug Administration
Published: 1990-11-21

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.. Device class: 2.

Clearance details

Applicant: Societa Gruppi Elastomeri S.A.
Product code: Code EZL
Device class: Class 2
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Date received: 1990-06-20
Decision date: 1990-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mendrisio, ES

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Recent devices under product code EZL

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K260756 — TraumaGuard Intra-Abdominal Pressure-Sensing System (000-0221)2026-09-04
K262056 — Rusch Latex Gold Foley Catheter2026-08-05
K252537 — Rusch SoftSimplastic Foley Catheters2026-01-20
K243011 — Silicone Urethral Catheter (Silicone Urethral Catheter)2025-06-16
K241424 — InnoCare Specialty Foley Catheter2024-09-18

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.