BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

    Dewin Blastocyst Medium (with HSA and without HSA)

    K Number: K231370 · Decision Aug 4, 2023
    View on FDA
    Classifications
    1
    FEI Numbers
    31
    Registration Numbers
    31
    Same Product Code
    258
    Applicant Total
    4
    Review Days
    84

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    Basic Information

    Device Name
    Dewin Blastocyst Medium (with HSA and without HSA)
    K Number
    K231370
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.6180
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Donnevie Medical Technology (Shanghai) Co. , Ltd.
    Date Received
    May 12, 2023
    Decision Date
    August 4, 2023
    Product Code
    MQL
    Advisory Committee
    Obstetrics/Gynecology
    Review Advisory Committee
    OB
    Third Party
    N

    Classifications

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

    Product Code Device Name
    MQL Media, Reproductive

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    Other Clearances by Donnevie Medical Technology (Shanghai) Co. , Ltd.

    K Number Device Name
    K251637 Dewin Reproductive Media (Dewin Gamete Buffer [with HSA and without HSA]; Dewin Follicle Flushing Solution, Dewin One Step medium [with HSA and without HSA])
    K242561 Dewin Reproductive Media (Dewin Vitrification Kit, Dewin Thawing Kit)
    K212426 Dewin Reproductive Media (Dewin Fertilization Medium [with HSA and without HSA] and Dewin Cleavage Medium [with HSA and without HSA])