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510(k) Data Aggregation

    K Number
    K952906
    Device Name
    THE TULIP LAPAROSCOPE SHEATH 6MM SINGLE STOPCOCK
    Manufacturer
    THE TULIP MFG. CO.
    Date Cleared
    1996-01-22

    (213 days)

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

    THE TULIP MFG. CO.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K952959
    Device Name
    THE TULIP LAPAROSCOPE SHEATH 6MM DUAL STOPCOCK
    Manufacturer
    THE TULIP MFG. CO.
    Date Cleared
    1996-01-22

    (210 days)

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

    THE TULIP MFG. CO.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K955501
    Device Name
    THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEP
    Manufacturer
    THE TULIP MFG. CO.
    Date Cleared
    1996-01-17

    (47 days)

    Product Code
    GEI
    Regulation Number
    878.4400
    Why did this record match?
    Applicant Name (Manufacturer) :

    THE TULIP MFG. CO.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K955502
    Device Name
    THE TULIP MONO POLAR ROTATABLE METZ SCISSORS
    Manufacturer
    THE TULIP MFG. CO.
    Date Cleared
    1996-01-17

    (47 days)

    Product Code
    GEI
    Regulation Number
    878.4400
    Why did this record match?
    Applicant Name (Manufacturer) :

    THE TULIP MFG. CO.

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

    Ask a specific question about this device

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