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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 a medical device manufactured by Beijing Zksk Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-06-06 under approval 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. It is manufactured by Beijing Zksk Technology Co., Ltd.. The 510(k) number is K213223.

When was Multi-Band Ligator approved by the FDA?

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

What company makes Multi-Band Ligator?

Multi-Band Ligator is manufactured by Beijing Zksk Technology Co., Ltd..

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

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

Other Devices by Beijing Zksk Technology Co., Ltd.

K213217Disposable hemoclip K213222Disposable Polypectomy Snare K213239Endoscopic Injection Needle K231721Disposable Hot Biopsy Forceps K242192Disposable Sphincterotome

Related Devices (Code: FHN)

K172985Ligation DeviceLeo Medical Co., Ltd.

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.

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