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510(k) Data Aggregation

    K Number
    K981989
    Device Name
    THE WAVE DIGITAL PHACO SYSTEM
    Manufacturer
    CIRCUIT TREE
    Date Cleared
    1998-08-25

    (81 days)

    Product Code
    HQC
    Regulation Number
    886.4670
    Why did this record match?
    Applicant Name (Manufacturer) :

    CIRCUIT TREE

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Phacoemulsification of cataracts in the human eye.
    Device Description
    Not Found
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    K Number
    K962430
    Device Name
    CTM REUSABLE PAK
    Manufacturer
    CIRCUIT TREE MEDICAL, INC.
    Date Cleared
    1996-07-23

    (29 days)

    Product Code
    HQC
    Regulation Number
    886.4670
    Why did this record match?
    Applicant Name (Manufacturer) :

    CIRCUIT TREE MEDICAL, INC

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
    Ask a Question
    K Number
    K962431
    Device Name
    CTM DISPOSABLE PAK
    Manufacturer
    CIRCUIT TREE MEDICAL, INC.
    Date Cleared
    1996-07-23

    (29 days)

    Product Code
    HQC
    Regulation Number
    886.4670
    Why did this record match?
    Applicant Name (Manufacturer) :

    CIRCUIT TREE MEDICAL, INC

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
    Ask a Question

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