BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    PRESSUREMATE MANUAL FEMORAL ACCESS COMPRESSION DEVICE

    K Number: K090286 · Decision Mar 23, 2009
    View on FDA
    Classifications
    1
    FEI Numbers
    186
    Registration Numbers
    186
    Same Product Code
    203
    Applicant Total
    8
    Review Days
    46

    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
    PRESSUREMATE MANUAL FEMORAL ACCESS COMPRESSION DEVICE
    K Number
    K090286
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.4450
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Advanced Vascular Dynamics
    Date Received
    February 5, 2009
    Decision Date
    March 23, 2009
    Product Code
    DXC
    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
    DXC Clamp, Vascular

    Similar 510(k) Clearances

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

    Fogarty Spring Clips, Handleless Clamps, and Clamp Inserts

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Arc Adjustable Radial Cuff Compression Device

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Life Saving Tourniquet

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial Restriction Clamp (ARC)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Namic Radial Arm Band, 23 cm (DYNJRADBAND); Namic Radial Arm Band, 26 cm (DYNJRADBANDL)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Radial Compression Device

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

    Other Clearances by Advanced Vascular Dynamics

    K Number Device Name
    K151363 Zephyr Vascular Compression Device
    K142122 RADAR VASCULAR COMPRESSION DEVICE
    K131571 AVD RIGHT RADIAL DRAPE
    K093192 FLOCHEC PHOTO PLETHYSMOGRAPHIC DEVICE
    K092503 RADAR VASCULAR COMPRESSION DEVICES
    K072167 COMFORTPRESS VASCULAR COMPRESSION ASSIST DEVICE
    K040615 COMPRESSAR SUPERCOMFORT DISC AND STRONGARM SUPERCOMFORT SYSTEM