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

    INNOFLUOR PHENOBARBITAL ASSAY SYSTEM

    K Number: K972330 · Decision Jul 14, 1997
    View on FDA
    Classifications
    1
    FEI Numbers
    4
    Registration Numbers
    4
    Same Product Code
    11
    Applicant Total
    11
    Review Days
    21

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    Basic Information

    Device Name
    INNOFLUOR PHENOBARBITAL ASSAY SYSTEM
    K Number
    K972330
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.3660
    Medical Specialty
    Clinical Toxicology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Oxis Intl., Inc.
    Date Received
    June 23, 1997
    Decision Date
    July 14, 1997
    Product Code
    LGQ
    Advisory Committee
    Clinical Toxicology
    Review Advisory Committee
    TX
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LGQ Fluorescence Polarization Immunoassay, Phenobarbital

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    Other Clearances by Oxis Intl., Inc.

    K Number Device Name
    K972331 INNOFLUOR GENTAMICIN ASSAY SYSTEM
    K970510 INNOFLOUR TOPIRAMATE REAGENT SET
    K970509 INNOFLOUR CALIBRATOR REAGENT SET
    K970517 INNOFLUOR TOPIRAMATE CONTROL SET
    K955568 INNOFLUOR QUINIDINE ASSAY SYSTEM
    K955570 INNOFLUOR AMIKACIN ASSAY SYSTEM
    K955569 INNOFLUOR GENTAMICIN ASSAY SYSTEM
    K955567 INNOFLUOR THEOPHYLLINE ASSAY SYSTEM
    K955562 INNOFLUOR PHENYTOIN ASSAY SYSTEM
    K950346 B-L RED(TM) DISCS
    Search all 11 clearances from Oxis Intl., Inc. →