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510(k) Data Aggregation

    K Number
    K000932
    Device Name
    ARACHNOPHLEBECTOMY NEEDLE
    Manufacturer
    ADVANCED MEDICAL PRODUCTS, INC.
    Date Cleared
    2000-05-17

    (55 days)

    Product Code
    GAH
    Regulation Number
    878.4800
    Why did this record match?
    Applicant Name (Manufacturer) :

    ADVANCED MEDICAL PRODUCTS, INC.

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