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

    ACS ANGIOTENSIN CONVERTING ENZYME (ACE) CALIBRATOR

    K Number: K930477 · Decision Jun 7, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    72
    Registration Numbers
    72
    Same Product Code
    129
    Applicant Total
    42
    Review Days
    129

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    Basic Information

    Device Name
    ACS ANGIOTENSIN CONVERTING ENZYME (ACE) CALIBRATOR
    K Number
    K930477
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1150
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Analytical Control Systems, Inc.
    Date Received
    January 29, 1993
    Decision Date
    June 7, 1993
    Product Code
    JIS
    Advisory Committee
    Clinical Chemistry
    Review Advisory Committee
    CH
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JIS Calibrator, Primary

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