MEMCATH UROLOGY CATHETER, MODEL 101 -000 - 006— 510(k) K993226

Name: FDA 510(k) clearance K993226
Creator: U.S. Food and Drug Administration
Published: 1999-12-10

Substantially Equivalent

Memcath Technologies, LLC

FDA 510(k) clearance K993226 for MEMCATH UROLOGY CATHETER, MODEL 101 -000 - 006, Substantially Equivalent on 1999-12-10. Applicant: Memcath Technologies, LLC. Device class: 2.

Clearance details

Applicant: Memcath Technologies, LLC
Product code: Code EZD
Device class: Class 2
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Date received: 1999-09-27
Decision date: 1999-12-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code EZD

product code EZD

Injury: 864
Malfunction: 2,210
Total: 3,074

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.