LogoFDA 510(k) Search
Search Filters

Search Results

Found 7 results

510(k) Data Aggregation

    K Number
    K003802
    Device Name
    HYSTEROSCOPES
    Manufacturer
    GLOBAL ENDOSCOPY, INC.
    Date Cleared
    2001-07-22

    (226 days)

    Product Code
    HIH
    Regulation Number
    884.1690
    Why did this record match?
    Applicant Name (Manufacturer) :

    GLOBAL ENDOSCOPY, INC.

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

    Ask a specific question about this device

    K Number
    K003805
    Device Name
    GYNECOLOGICAL LAPAROSCOPES
    Manufacturer
    GLOBAL ENDOSCOPY, INC.
    Date Cleared
    2001-07-22

    (226 days)

    Product Code
    HET
    Regulation Number
    884.1720
    Why did this record match?
    Applicant Name (Manufacturer) :

    GLOBAL ENDOSCOPY, INC.

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

    Ask a specific question about this device

    K Number
    K003831
    Device Name
    ARTHROSCOPES
    Manufacturer
    GLOBAL ENDOSCOPY, INC.
    Date Cleared
    2001-07-20

    (221 days)

    Product Code
    HRX
    Regulation Number
    888.1100
    Why did this record match?
    Applicant Name (Manufacturer) :

    GLOBAL ENDOSCOPY, INC.

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

    Ask a specific question about this device

    K Number
    K003830
    Device Name
    ENT ENDOSCOPES
    Manufacturer
    GLOBAL ENDOSCOPY, INC.
    Date Cleared
    2001-04-09

    (119 days)

    Product Code
    EOB
    Regulation Number
    874.4760
    Why did this record match?
    Applicant Name (Manufacturer) :

    GLOBAL ENDOSCOPY, INC.

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

    Ask a specific question about this device

    K Number
    K003803
    Device Name
    GENERAL SURGICAL LAPAROSCOPES
    Manufacturer
    GLOBAL ENDOSCOPY, INC.
    Date Cleared
    2001-03-07

    (89 days)

    Product Code
    GCJ
    Regulation Number
    876.1500
    Why did this record match?
    Applicant Name (Manufacturer) :

    GLOBAL ENDOSCOPY, INC.

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

    Ask a specific question about this device

    K Number
    K003806
    Device Name
    URETEROSCOPES
    Manufacturer
    GLOBAL ENDOSCOPY, INC.
    Date Cleared
    2001-02-22

    (76 days)

    Product Code
    FGB
    Regulation Number
    876.1500
    Why did this record match?
    Applicant Name (Manufacturer) :

    GLOBAL ENDOSCOPY, INC.

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

    Ask a specific question about this device

    K Number
    K003807
    Device Name
    CYSTOSCOPES
    Manufacturer
    GLOBAL ENDOSCOPY, INC.
    Date Cleared
    2001-02-22

    (76 days)

    Product Code
    FAJ
    Regulation Number
    876.1500
    Why did this record match?
    Applicant Name (Manufacturer) :

    GLOBAL ENDOSCOPY, INC.

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

    Ask a specific question about this device

    Page 1 of 1