Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

RightLance Blood Lancing System

K-Number: K222034 · 2022-09-07

Decision Date2022-09-07
Product CodeQRL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RightLance Blood Lancing System is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Ruicheng Medical Supplies Co., Ltd.. It received FDA 510(k) clearance on 2022-09-07 under 510(k) 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. The listed applicant is Beijing Ruicheng Medical Supplies Co., Ltd.. The 510(k) number is K222034.

When did RightLance Blood Lancing System receive FDA 510(k) clearance?

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

Who is the listed applicant for RightLance Blood Lancing System?

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

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

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

Other records listing Beijing Ruicheng Medical Supplies Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: QRL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.