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

    NEXSTAT PLUS AND NEXFOAM PLUS TOPICAL HEMOSTAT DRESSING

    K Number: K122886 · Decision Nov 15, 2012
    View on FDA
    Classifications
    1
    FEI Numbers
    113
    Registration Numbers
    113
    Same Product Code
    126
    Applicant Total
    10
    Review Days
    56

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    Basic Information

    Device Name
    NEXSTAT PLUS AND NEXFOAM PLUS TOPICAL HEMOSTAT DRESSING
    K Number
    K122886
    Device Class
    FDA unclassified
    Clearance Type
    Special
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Hemostasis, LLC
    Date Received
    September 20, 2012
    Decision Date
    November 15, 2012
    Product Code
    QSY
    Advisory Committee
    Unknown
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    QSY Hemostatic Wound Dressing Without Thrombin Or Other Biologics

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    Other Clearances by Hemostasis, LLC

    K Number Device Name
    K234131 Resolv Endoscopic Hemostat System
    K220326 PosiSep X BAM Hemostat Dressing/Intranasal Splint
    K210411 PosiSep EAR Fragmentable Ear Dressing
    K142348 OsteoSeal Bone Hemostat
    K122494 POSISEP AND POSISEP X HEMOSTAT DRESSING/INTRANASAL SPLINT
    K120958 POSISEP AND POSISEP X HEMOSTAT DRESSINGS
    K102459 NEXSTAT (TM) TOPICAL HEMOSTAT POWDER; NEXFOAM (R) TOPICAL SPONGE
    K072900 EXCELARREST FOAM
    K070211 TRAUMARREST AND BLEEDARREST HEMOSTATIC PARTICLES AND FOAM