MagiCath II— 510(k) K210929

Name: FDA 510(k) clearance K210929
Creator: U.S. Food and Drug Administration
Published: 2022-09-13

Substantially Equivalent

Woo Young Medical Co., Ltd.

FDA 510(k) clearance K210929 for MagiCath II, Substantially Equivalent on 2022-09-13. Applicant: Woo Young Medical Co., Ltd.. Device class: 2.

Clearance details

Applicant: Woo Young Medical Co., Ltd.
Product code: Code FOZ
Device class: Class 2
Regulation: 21 CFR 880.5200
Advisory panel: General Hospital
Date received: 2021-03-29
Decision date: 2022-09-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jincheon-Gun, KR

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FOZ

product code FOZ

Death: 38
Injury: 2,290
Malfunction: 25,858
Other: 11
Total: 28,197

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.