RightLance Blood Lancing System— 510(k) K222034

Name: FDA 510(k) clearance K222034
Creator: U.S. Food and Drug Administration
Published: 2022-09-07

Substantially Equivalent

Beijing Ruicheng Medical Supplies Co., Ltd.

FDA 510(k) clearance K222034 for RightLance Blood Lancing System, Substantially Equivalent on 2022-09-07. Applicant: Beijing Ruicheng Medical Supplies Co., Ltd.. Device class: 2.

Clearance details

Applicant: Beijing Ruicheng Medical Supplies Co., Ltd.
Product code: Code QRL
Device class: Class 2
Regulation: 21 CFR 878.4850
Advisory panel: General, Plastic Surgery
Date received: 2022-07-11
Decision date: 2022-09-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Beijing, CN

Download summary PDF View on FDA.gov ↗

Recent devices under product code QRL

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K262135 — Lancing device2026-08-18
K262211 — Lancet2026-07-22
K260122 — Lancing Device (PressGo, LDE3, LDE3AST, LDE5, EasyStep)2026-07-06
K253706 — Lancing device (HH-XV-T)2025-12-09
K250813 — MICROLET®NEXT 2 Lancing Device2025-05-14

More clearances from Beijing Ruicheng Medical Supplies Co., Ltd.

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K222408 — Disposable Safety Lancet2022-11-29

Adverse events under product code QRL

product code QRL

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.