BEUDAMED
    FDA 510(k) Unknown 🇺🇸 United States

    TENS-O-TEST

    K Number: K781321 · Decision Jul 31, 1978
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    2
    Review Days
    —

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    Basic Information

    Device Name
    TENS-O-TEST
    K Number
    K781321
    Clearance Type
    Traditional
    Decision
    Unknown
    Applicant
    Curomatic, Inc.
    Date Received
    July 31, 1978
    Decision Date
    July 31, 1978
    Advisory Committee
    Unknown
    Review Advisory Committee
    CV
    Third Party
    N

    Other Clearances by Curomatic, Inc.

    K Number Device Name
    K791637 TENS-O-TEST