Multi-Band Ligator— 510(k) K213223

Name: FDA 510(k) clearance K213223
Creator: U.S. Food and Drug Administration
Published: 2022-06-06

Substantially Equivalent

Beijing Zksk Technology Co., Ltd.

FDA 510(k) clearance K213223 for Multi-Band Ligator, Substantially Equivalent on 2022-06-06. Applicant: Beijing Zksk Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Beijing Zksk Technology Co., Ltd.
Product code: Code FHN
Device class: Class 2
Regulation: 21 CFR 876.4400
Advisory panel: Gastroenterology, Urology
Date received: 2021-09-29
Decision date: 2022-06-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Beijing, CN

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.