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

    QUICKPAD (ALCOHOL SWABS)

    K Number: K892193 · Decision Aug 4, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    113
    Registration Numbers
    113
    Same Product Code
    24
    Applicant Total
    1
    Review Days
    121

    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
    QUICKPAD (ALCOHOL SWABS)
    K Number
    K892193
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Applicant
    Holtsch Co., Inc.
    Date Received
    April 5, 1989
    Decision Date
    August 4, 1989
    Product Code
    LKB
    Advisory Committee
    Unknown
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LKB Pad, Alcohol, Device Disinfectant

    Similar 510(k) Clearances

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

    PREVANTICS DEVICE SWAB

    FDA 510(k)
    FDA Unclassified ·Unknown

    BD ALCOHOL SWAB

    FDA 510(k)
    FDA Unclassified ·Unknown

    SITESCRUB IPA DEVICE

    FDA 510(k)
    FDA Unclassified ·Unknown

    I.V. STARR KIT

    FDA 510(k)
    FDA Unclassified ·Unknown

    STERI-SWAB

    FDA 510(k)
    FDA Unclassified ·Unknown

    HEXIDIS ALCOHOL SWAB

    FDA 510(k)
    FDA Unclassified ·Unknown
    View all