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FDA 510(k)

Disposable Blood Lancets

K-Number: K223314 · 2023-01-25

ApplicantHuaian Hening Medical Instruments Co., Ltd.
Decision Date2023-01-25
Product CodeQRK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Disposable Blood Lancets is a medical device manufactured by Huaian Hening Medical Instruments Co., Ltd.. It received FDA 510(k) clearance on 2023-01-25 under approval number K223314. The device is classified under product code QRK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Disposable Blood Lancets?

Disposable Blood Lancets is a medical device that received FDA 510(k) clearance on 2023-01-25. It is manufactured by Huaian Hening Medical Instruments Co., Ltd.. The 510(k) number is K223314.

When was Disposable Blood Lancets approved by the FDA?

Disposable Blood Lancets received FDA 510(k) clearance on 2023-01-25, under approval number K223314.

What company makes Disposable Blood Lancets?

Disposable Blood Lancets is manufactured by Huaian Hening Medical Instruments Co., Ltd..

What is the FDA product code for Disposable Blood Lancets?

The FDA product code for Disposable Blood Lancets is QRK.

Related Clinical Trials

NCT07273877 "Real-world Assessment of BP Control in Patients With Hypertension by the Netrod RDN System" - REACH-RDN ENROLLING_BY_INVITATION

Other Devices by Huaian Hening Medical Instruments Co., Ltd.

K223313Disposable Safety Lancets

Related Devices (Code: QRK)

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Official Source

View on FDA Database →

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

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