Disposable Blood Lancet (4 models)— 510(k) K244031
Substantially EquivalentSteriLance Medical (Suzhou), Inc.
FDA 510(k) clearance K244031 for Disposable Blood Lancet (4 models), Substantially Equivalent on 2025-02-26. Applicant: SteriLance Medical (Suzhou), Inc.. Device class: 2.
Clearance details
- Device name as filed
- Disposable Blood Lancet (Soft Pro); Disposable Blood Lancet (Softsure); Disposable Blood Lancet (Softsure Pro); Disposable Blood Lancet (Softsense)
- Applicant
- SteriLance Medical (Suzhou), Inc.
- Product code
- Code QRK
- Device class
- Class 2
- Regulation
- 21 CFR 878.4850
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Suzhou, CN
Recent devices under product code QRK
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