Urethrotech UCD— 510(k) K190060

Name: FDA 510(k) clearance K190060
Creator: U.S. Food and Drug Administration
Published: 2019-10-04

Substantially Equivalent

Urethrotech

FDA 510(k) clearance K190060 for Urethrotech UCD, Substantially Equivalent on 2019-10-04. Applicant: Urethrotech. Device class: 2.

Clearance details

Applicant: Urethrotech
Product code: Code EZL
Device class: Class 2
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Date received: 2019-01-11
Decision date: 2019-10-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kingston Upon Thames, GB

Download summary PDF View on FDA.gov ↗

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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.