BEUDAMED
    FDA 510(k) Substantially Equivalent 🇺🇸 United States

    CARDIOVIT CS-100

    K Number: K914970 · Decision Nov 3, 1992
    View on FDA
    Classifications
    0
    FEI Numbers
    11
    Registration Numbers
    11
    Same Product Code
    82
    Applicant Total
    10
    Review Days
    364

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    Basic Information

    Device Name
    CARDIOVIT CS-100
    K Number
    K914970
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Schiller America, Inc.
    Date Received
    November 5, 1991
    Decision Date
    November 3, 1992
    Product Code
    LOS
    Advisory Committee
    Unknown
    Review Advisory Committee
    CV
    Third Party
    N

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    Other Clearances by Schiller America, Inc.

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    K973751 MT-200
    K970879 CARDIOVIT CS-200
    K953396 CARDIOVIT AT-1C, AT-2C
    K954066 MINISCOPE MS-3
    K941462 CARDIOVIT AT-5C
    K946205 CARDIOVIT AT-1, P-80
    K896121 SCHILLER MODEL SP-200 SPIROVIT(TM)
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