BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    AC-901 I.V. INFUSION DROP COUNTER

    K Number: K923561 · Decision May 26, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    3
    Registration Numbers
    3
    Same Product Code
    38
    Applicant Total
    2
    Review Days
    313

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    Basic Information

    Device Name
    AC-901 I.V. INFUSION DROP COUNTER
    K Number
    K923561
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.2420
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Lamtic, Inc.
    Date Received
    July 17, 1992
    Decision Date
    May 26, 1993
    Product Code
    FLN
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    FLN Monitor, Electric For Gravity Flow Infusion Systems

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    Other Clearances by Lamtic, Inc.

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