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

    ALIZARIN SULFONATE, CALCIUM

    K Number: K801290 · Decision Jun 30, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    1
    Applicant Total
    69
    Review Days
    31

    Basic Information

    Device Name
    ALIZARIN SULFONATE, CALCIUM
    K Number
    K801290
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1145
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    UNION CARBIDE CORP.
    Date Received
    May 30, 1980
    Decision Date
    June 30, 1980
    Product Code
    CID
    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
    CID Alizarin Sulfonate, Calcium

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (CID), ordered by most recent decision date.

    KODAK EKTACHEM DT SLIDES (CA)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry
    View all

    Other Clearances by UNION CARBIDE CORP.

    K Number Device Name
    K830337 MARK III OXYGEN WALKER SYS-LOW PRESS
    K820836 MARK III OXYGEN WALKER SYSTEM
    K820535 LASER GAS MIXTURES
    K812536 LINDE MARK II
    K810732 LINDE MARK II OXYGEN RESERV. TYPE OR-4
    K810596 CENTRIFI CHEM SYSTEM 400 ANALYZER
    K810129 CENTRIFICHEM SYSTEM 500
    K803216 CENTRIFICHEM AST/SGOT OPTIMIZED REAGENT
    K802741 CENTRIFICHEM COMB. SERUM-BASED CALIB.
    K802520 CENTRIFICHEM PIPETTOR ACCURACY CALIB.
    Search all 69 clearances from UNION CARBIDE CORP. →