BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent for Some Indications 🇺🇸 United States

    SPORICIDIN BRAND DISINFECT TOWELETTES/SPRAY/SOLUT

    K Number: K922262 · Decision Sep 15, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    370
    Registration Numbers
    370
    Same Product Code
    72
    Applicant Total
    8
    Review Days
    126

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    Basic Information

    Device Name
    SPORICIDIN BRAND DISINFECT TOWELETTES/SPRAY/SOLUT
    K Number
    K922262
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.6890
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent for Some Indications
    Applicant
    Sporicidin Intl.
    Date Received
    May 12, 1992
    Decision Date
    September 15, 1992
    Product Code
    LRJ
    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
    LRJ Disinfectant, Medical Devices

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    Other Clearances by Sporicidin Intl.

    K Number Device Name
    K003087 MODIFICATION TO SPORICIDIN STERILIZING AND DISINFECTING SOLUTION
    K983194 SPORICIDIN STERILIZING AND DISINFECTING SOLUTION (SSDS)
    K926013 SPORICIDIN BRAND DISINFECT TOWEL, SPRAY/SOLUT MODI
    K904581 SPORICIDIN BRAND DISINFECTANT SOLUTION
    K904580 SPORICIDIN BRAND DISINFECTANT SPRAY
    K904579 SPORICIDIN BRAND DISINFECTANT TOWELETTES
    K830722 SPORIDIDIN-D COLD STERILIZING/SOLUTION