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

    SUTURE REMOVAL KIT

    K Number: K810685 · Decision Mar 26, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    444
    Registration Numbers
    445
    Same Product Code
    103
    Applicant Total
    8
    Review Days
    13

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    Basic Information

    Device Name
    SUTURE REMOVAL KIT
    K Number
    K810685
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Medical Action Industries, Inc.
    Date Received
    March 13, 1981
    Decision Date
    March 26, 1981
    Product Code
    GEN
    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
    GEN Forceps, General & Plastic Surgery

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    Other Clearances by Medical Action Industries, Inc.

    K Number Device Name
    K042526 DRAPE, SURGICAL, X-RAY ELEMENT, MODELS NON STERILE 6120-00, STERILE 704-B, NON STERILE 6124-00X, STERILE 704-BX
    K042527 SPATULA, CERVICAL, CYTOLOGICAL, MODEL 22-9107
    K022948 VAGINAL SPECULUM, MODEL 5555S, 5555M, OR 5555L
    K946019 SURGICLA INSTRUMENT KIT
    K923846 BURN DRESSING
    K884826 GAUZE SPONGE
    K810184 LAPAROTOMY SPONGE