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510(k) Data Aggregation

    K Number
    K970272
    Device Name
    PATIENT RESTRAINT
    Manufacturer
    FLA. ORTHOPEDICS, INC.
    Date Cleared
    1997-04-11

    (78 days)

    Product Code
    FMQ
    Regulation Number
    880.6760
    Why did this record match?
    Applicant Name (Manufacturer) :

    FLA. ORTHOPEDICS, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K970273
    Device Name
    PATIENT RESTRAINTS
    Manufacturer
    FLA. ORTHOPEDICS, INC.
    Date Cleared
    1997-04-11

    (78 days)

    Product Code
    FMQ
    Regulation Number
    880.6760
    Why did this record match?
    Applicant Name (Manufacturer) :

    FLA. ORTHOPEDICS, 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
    K970274
    Device Name
    PATIENT RESTRAINTS
    Manufacturer
    FLA. ORTHOPEDICS, INC.
    Date Cleared
    1997-04-11

    (78 days)

    Product Code
    FMQ
    Regulation Number
    880.6760
    Why did this record match?
    Applicant Name (Manufacturer) :

    FLA. ORTHOPEDICS, 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
    K970275
    Device Name
    PATIENT RESTRAINTS
    Manufacturer
    FLA. ORTHOPEDICS, INC.
    Date Cleared
    1997-04-11

    (78 days)

    Product Code
    FMQ
    Regulation Number
    880.6760
    Why did this record match?
    Applicant Name (Manufacturer) :

    FLA. ORTHOPEDICS, INC.

    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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