FDA 510(k)

Multi-Band Ligator

K-Number: K213223 · 2022-06-06

ApplicantBeijing Zksk Technology Co., Ltd.

Decision Date2022-06-06

Product CodeFHN

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

Multi-Band Ligator is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Zksk Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-06-06 under 510(k) number K213223. The device is classified under product code FHN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Multi-Band Ligator?

Multi-Band Ligator is a medical device that received FDA 510(k) clearance on 2022-06-06. The listed applicant is Beijing Zksk Technology Co., Ltd.. The 510(k) number is K213223.

When did Multi-Band Ligator receive FDA 510(k) clearance?

Multi-Band Ligator received FDA 510(k) clearance on 2022-06-06, under 510(k) number K213223.

Who is the listed applicant for Multi-Band Ligator?

The FDA 510(k) record lists Beijing Zksk Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Multi-Band Ligator?

The FDA product code for Multi-Band Ligator is FHN.

Other records listing Beijing Zksk Technology Co., Ltd. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.