LogoFDA 510(k) Search
Search Filters

Search Results

Found 7 results

510(k) Data Aggregation

    K Number
    K000619
    Device Name
    SCANDINAVIAN IVF SCIENCES AB, G2.2
    Manufacturer
    VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB
    Date Cleared
    2000-06-27

    (131 days)

    Product Code
    MQL
    Regulation Number
    884.6180
    Why did this record match?
    Applicant Name (Manufacturer) :

    VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
    Ask a Question
    K Number
    K000627
    Device Name
    SCANDINAVIAN IVF SCIENCES AB, HYBASE-1
    Manufacturer
    VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB
    Date Cleared
    2000-06-13

    (117 days)

    Product Code
    MQL
    Regulation Number
    884.6180
    Why did this record match?
    Applicant Name (Manufacturer) :

    VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
    Ask a Question
    K Number
    K000625
    Device Name
    SCANDINAVIAN IVF SCIENCES AB, G1.2
    Manufacturer
    VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB
    Date Cleared
    2000-05-23

    (96 days)

    Product Code
    MQL
    Regulation Number
    884.6180
    Why did this record match?
    Applicant Name (Manufacturer) :

    VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
    Ask a Question
    K Number
    K000626
    Device Name
    SCANDINAVIAN IVF SCIENCES AB, GAMETE-100
    Manufacturer
    VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB
    Date Cleared
    2000-05-23

    (96 days)

    Product Code
    MQL
    Regulation Number
    884.6180
    Why did this record match?
    Applicant Name (Manufacturer) :

    VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
    Ask a Question
    K Number
    K000618
    Device Name
    SCANDINAVIAN IVF SCIENCES AB, THAW-KIT 1
    Manufacturer
    VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB
    Date Cleared
    2000-05-17

    (90 days)

    Product Code
    MQL
    Regulation Number
    884.6180
    Why did this record match?
    Applicant Name (Manufacturer) :

    VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
    Ask a Question
    K Number
    K000621
    Device Name
    SCANDINAVIAN IVF SCIENCES AB, SPERMRINSE -20/100
    Manufacturer
    VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB
    Date Cleared
    2000-05-16

    (89 days)

    Product Code
    MQL
    Regulation Number
    884.6180
    Why did this record match?
    Applicant Name (Manufacturer) :

    VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
    Ask a Question
    K Number
    K000623
    Device Name
    SCANDINAVIAN IVF SCIENCES AB, FREEZE-KIT 1
    Manufacturer
    VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB
    Date Cleared
    2000-05-16

    (89 days)

    Product Code
    MQL
    Regulation Number
    884.6180
    Why did this record match?
    Applicant Name (Manufacturer) :

    VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB

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

    Page 1 of 1