BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    TECNOL SECURE-ALL PELVIC TRACTION BELT

    K Number: K882640 · Decision Jul 27, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    115
    Registration Numbers
    115
    Same Product Code
    10
    Applicant Total
    35
    Review Days
    30

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    Basic Information

    Device Name
    TECNOL SECURE-ALL PELVIC TRACTION BELT
    K Number
    K882640
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    888.5890
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Applicant
    Tecnol New Jersey Wound Care, Inc.
    Date Received
    June 27, 1988
    Decision Date
    July 27, 1988
    Product Code
    KQZ
    Advisory Committee
    Orthopedic
    Review Advisory Committee
    OR
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KQZ Component, Traction, Non-Invasive

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    Other Clearances by Tecnol New Jersey Wound Care, Inc.

    K Number Device Name
    K913043 MODIFICATION TECNOL FLUIDSHIELD SURGICAL MASKS
    K911891 FLUIDSHIELD(TM) CONE CLASSIC(TM) II SURGICAL MASK
    K911907 FLUIDSHIELD CONE CLASSIC II SURG MASK W/SPLASH VIS
    K896193 TECNOL LAZER(TM) SURGICAL MASK
    K894205 TECNOL SILK STRIP
    K893702 TECNOL GAITERS PRODUCT NUMBER 47725-010
    K891187 TECNOL NASO-GASTRIC TUBE HOLDER
    K891178 TECNOL SECURE-ALL TUBE HOLDER
    K884440 TECNOL VARIABLE TENSION BANDAGE
    K882641 TECNOL CATHETER LEG STRAP
    Search all 35 clearances from Tecnol New Jersey Wound Care, Inc. →