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FDA 510(k)

Disposable Safety Lancets

K-Number: K221778 · 2022-10-03

Decision Date2022-10-03
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Disposable Safety Lancets is a medical device manufactured by Suzhou Kyuan Medical Apparatus Co., Ltd.. It received FDA 510(k) clearance on 2022-10-03 under approval number K221778. The device is classified under product code FMK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Disposable Safety Lancets?

Disposable Safety Lancets is a medical device that received FDA 510(k) clearance on 2022-10-03. It is manufactured by Suzhou Kyuan Medical Apparatus Co., Ltd.. The 510(k) number is K221778.

When was Disposable Safety Lancets approved by the FDA?

Disposable Safety Lancets received FDA 510(k) clearance on 2022-10-03, under approval number K221778.

What company makes Disposable Safety Lancets?

Disposable Safety Lancets is manufactured by Suzhou Kyuan Medical Apparatus Co., Ltd..

What is the FDA product code for Disposable Safety Lancets?

The FDA product code for Disposable Safety Lancets is FMK.

Related Clinical Trials

Other Devices by Suzhou Kyuan Medical Apparatus Co., Ltd.

Related Devices (Code: FMK)

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.