BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

    Lancing System, Sterile Lancet for Single Use, Lancing Device

    K Number: K222472 · Decision Nov 30, 2022
    View on FDA
    Classifications
    1
    FEI Numbers
    84
    Registration Numbers
    84
    Same Product Code
    23
    Applicant Total
    2
    Review Days
    106

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    Lancing System, Sterile Lancet for Single Use, Lancing Device
    K Number
    K222472
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4850
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Shandong Lianfa Medical Plastic Products Co. , Ltd.
    Date Received
    August 16, 2022
    Decision Date
    November 30, 2022
    Product Code
    QRL
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    QRL Multiple Use Blood Lancet For Single Patient Use Only

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (QRL), ordered by most recent decision date.

    Lancing device (HH-XV-T)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MICROLET®NEXT 2 Lancing Device

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Lancet (IA, IB, IC, ID, IE, IK, IL, IM, IIA, IIB, III, V, VI, VII, VIII, IX); Lancing device (HH-X-T, HH-XV-T, HH-XVI-T, HH-XVII-T, HH-XVIII-T, HH-XIX, HH-XXI-T, HH-XXII-T, HH-XXIII-T, HH-XXIV-T, HH-XXV-T, HH-XXVI-T, HH-XXVIII-T, HH-XXIX-T, HH-XXX-T, HH-XIII-T, HH-XXVII-T)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Facet Aurora Reusable Lancet Base

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Medifun Lancing Device, Model No. LD-E1

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Verifine® Ease Lancing Device, Verifine® Lancing Device

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery
    View all

    Other Clearances by Shandong Lianfa Medical Plastic Products Co. , Ltd.

    K Number Device Name
    K222376 Lianfa Safety Lancet (Five Models: NPA, PA, PA2, TPA, and APA)