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

    ALRAND INC. (DENTAL HAND INSTRUMENTS)

    K Number: K926190 · Decision Jan 18, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    92
    Registration Numbers
    92
    Same Product Code
    10
    Applicant Total
    1
    Review Days
    405

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    Basic Information

    Device Name
    ALRAND INC. (DENTAL HAND INSTRUMENTS)
    K Number
    K926190
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.3150
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Alrand, Inc.
    Date Received
    December 9, 1992
    Decision Date
    January 18, 1994
    Product Code
    EJP
    Advisory Committee
    Dental
    Review Advisory Committee
    DE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    EJP Articulators

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