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510(k) Data Aggregation

    K Number
    K001314
    Device Name
    MEDSCOPE
    Manufacturer
    ALL-PRO IMAGING CORP.
    Date Cleared
    2000-07-25

    (90 days)

    Product Code
    HEX
    Regulation Number
    884.1630
    Why did this record match?
    Applicant Name (Manufacturer) :

    ALL-PRO IMAGING CORP.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K001321
    Device Name
    ALL-PRO 2010
    Manufacturer
    ALL-PRO IMAGING CORP.
    Date Cleared
    2000-05-16

    (20 days)

    Product Code
    IXW
    Regulation Number
    892.1900
    Why did this record match?
    Applicant Name (Manufacturer) :

    ALL-PRO IMAGING CORP.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K991435
    Device Name
    AII-PRO 100 PLUS AND ALL-PRO 200
    Manufacturer
    ALL-PRO IMAGING CORP.
    Date Cleared
    1999-05-20

    (24 days)

    Product Code
    IXW
    Regulation Number
    892.1900
    Why did this record match?
    Applicant Name (Manufacturer) :

    ALL-PRO IMAGING CORP.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    The All-Pro 100 Plus and All-Pro 200 are automatic x-ray film processors. They develop, fix, wash and dry medical x-ray film. Properly processed x-ray films are available for reading by medical practitioners more rapidly and with more consistency than with manual processing.
    Device Description
    automatic x-ray film processors
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