Lancing device
FDA 510(k) K221970 · SteriLance Medical (Suzhou), Inc.
510(k) numberK221970
Submission
- Device name
- Lancing device
- Applicant
- SteriLance Medical (Suzhou), Inc.
Suzhou, CN - Received
- July 5, 2022
- Decision date
- August 30, 2022
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- QRL – Multiple Use Blood Lancet For Single Patient Use Only
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4850
- Specialty
- General, Plastic Surgery
A multiple use capable blood lancet intended for use on a single patient that is comprised of a single use blade attached to a solid, reusable base that is used to puncture the skin to obtain a drop of blood for diagnostic purposes.
Other 510(k)s with product code QRL
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262135 | Lancing deviceQRL · Traditional | Tianjin Huahong Technology Co., Ltd. | 08/18/2026SE |
| K262211 | LancetQRL · Special | Tianjin Huahong Technology Co., Ltd. | 07/22/2026SE |
| K260122 | Lancing Device (PressGo, LDE3, LDE3AST, LDE5, EasyStep)QRL · Traditional | SteriLance Medical (Suzhou), Inc. | 07/06/2026SE |
| K253706 | Lancing device (HH-XV-T)QRL · Special | Tianjin Huahong Technology Co., Ltd. | 12/09/2025SE |
| K250813 | MICROLET®NEXT 2 Lancing DeviceQRL · Traditional | Ascensia Diabetes Care U.S., Inc. | 05/14/2025SE |
| K243306 | Lancet (IA, IB, IC, ID, IE, IK, IL, IM, IIA, IIB, III, V, VI, VII, VIII, IX); Lancing…QRL · Special | Tianjin Huahong Technology Co., Ltd. | 11/15/2024SE |
| K232912 | Facet Aurora Reusable Lancet BaseQRL · Traditional | Facet Technologies, LLC | 01/25/2024SE |
| K231797 | Medifun Lancing Device, Model No. LD-E1QRL · Traditional | Medifun Corporation | 11/22/2023SE |
| K223643 | Verifine® Ease Lancing Device, Verifine® Lancing DeviceQRL · Traditional | Promisemed Hangzhou Meditech Co., Ltd. | 02/21/2023SE |
| K221419 | TD-5010 Lancing Device and TD-5084 Sterile LancetsQRL · Traditional | Gostar Co., Ltd. | 01/20/2023SE |
More from Gostar Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K262631 | Disposable blood lancet (Soft Pro, Softsure, Softsure Pro, Softsense)QRK · Special | 08/25/2026SE |
| K260122 | Lancing Device (PressGo, LDE3, LDE3AST, LDE5, EasyStep)QRL · Traditional | 07/06/2026SE |
| K261634 | Disposable Blood Lancet (Soft)QRK · Special | 06/12/2026SE |
| K244036 | Heel Incision Safety Lancet (SteriHeel 2)FMK · Traditional | 02/26/2025SE |
| K244031 | Disposable Blood Lancet (Soft Pro); Disposable Blood Lancet (Softsure); Disposable Blood…QRK · Traditional | 02/26/2025SE |
| K233796 | Disposable safety lancet (Impress); Disposable safety lancet (Impress Pro); Disposable…FMK · Traditional | 01/16/2024SE |
| K221521 | Disposable Safety LancetFMK · Traditional | 10/28/2022SE |
| K221507 | Disposable Blood LancetQRK · Traditional | 08/31/2022SE |
| K210745 | Heel Incision Safety LancetFMK · Traditional | 08/26/2021SE |
| K153706 | Insulin Pen NeedleFMI · Traditional | 08/29/2016SE |
Questions and answers
When was Lancing device cleared by the FDA?
Lancing device (K221970) received a 510(k) decision of Substantially Equivalent on August 30, 2022, 56 days after the submission was received.
What is the product code of K221970?
The FDA product code is QRL – Multiple Use Blood Lancet For Single Patient Use Only, a Class II (moderate risk) device regulated under 21 CFR 878.4850.