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FDA 510(k)

RightLance Blood Lancing System

K-Number: K222034 · 2022-09-07

ApplicantBeijing Ruicheng Medical Supplies Co., Ltd.
Decision Date2022-09-07
Product CodeQRL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RightLance Blood Lancing System is a medical device manufactured by Beijing Ruicheng Medical Supplies Co., Ltd.. It received FDA 510(k) clearance on 2022-09-07 under approval number K222034. The device is classified under product code QRL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RightLance Blood Lancing System?

RightLance Blood Lancing System is a medical device that received FDA 510(k) clearance on 2022-09-07. It is manufactured by Beijing Ruicheng Medical Supplies Co., Ltd.. The 510(k) number is K222034.

When was RightLance Blood Lancing System approved by the FDA?

RightLance Blood Lancing System received FDA 510(k) clearance on 2022-09-07, under approval number K222034.

What company makes RightLance Blood Lancing System?

RightLance Blood Lancing System is manufactured by Beijing Ruicheng Medical Supplies Co., Ltd..

What is the FDA product code for RightLance Blood Lancing System?

The FDA product code for RightLance Blood Lancing System is QRL.

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Related PubMed Literature

PMID: 41336744 From laboratory to pre-market prototyping: lessons learned from a noninvasive blood glucose level measurement device. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference (2025)

Other Devices by Beijing Ruicheng Medical Supplies Co., Ltd.

K222408Disposable Safety Lancet

Related Devices (Code: QRL)

K222472Lancing System, Sterile Lancet for Single Use, Lancing DeviceShandong Lianfa Medical Plastic Products Co. , Ltd. K223099Facet Manatee Reusable Lancing BaseFacet Technologies, LLC K222656LDE4 Lancing DeviceI-Sens, Inc. K222246Disposable Sterile LancetTianjin Rilifine Medical Device Co., Ltd. K222539Facet Blood LancetsFacet Technologies, LLC K221072TRUEdraw Lancing Device, Mini Lancing DeviceTrividia Health

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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