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

    Compression Therapy Device (LGT-2202DVT)

    K Number: K250242 · Decision Apr 24, 2026
    View on FDA
    Classifications
    1
    FEI Numbers
    129
    Registration Numbers
    129
    Same Product Code
    349
    Applicant Total
    3
    Review Days
    452

    Basic Information

    Device Name
    Compression Therapy Device (LGT-2202DVT)
    K Number
    K250242
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.5800
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Guangzhou Longest Medical Technology Co., Ltd.
    Date Received
    January 27, 2025
    Decision Date
    April 24, 2026
    Product Code
    JOW
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JOW Sleeve, Limb, Compressible

    Similar 510(k) Clearances

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

    NanoPress 760A-BT (760A-BT)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Bio Arterial Deluxe (IC-BAP-DX)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Sequential Compression System (SCD600)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VenAir, Sequential Compression System (9P-089000); VenAir, Sequential Compression System (PM01D01 / Calf garment (S)); VenAir, Sequential Compression System (PM01E01 / Calf garment (M)); VenAir, Sequential Compression System (PM01F01 / Calf garment (L)); VenAir, Sequential Compression System (PM01G01 / Thigh garment (S)); VenAir, Sequential Compression System (PM01H01 / Thigh garment (M)); VenAir, Sequential Compression System (PM01I01 / Thigh garment (L)); VenAir, Sequential Compr

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PlasmaFlow X Compression Sleeve Device (XPF0001)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PnueAira (PNCU-01)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular
    View all

    Other Clearances by Guangzhou Longest Medical Technology Co., Ltd.

    K Number Device Name
    K252154 Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP)
    K250244 Compression Therapy Device (LGT-2210DS)