BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

    One Step Pregnancy Test

    K Number: K210341 · Decision Mar 10, 2022
    View on FDA
    Classifications
    1
    FEI Numbers
    117
    Registration Numbers
    117
    Same Product Code
    225
    Applicant Total
    4
    Review Days
    398

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    Basic Information

    Device Name
    One Step Pregnancy Test
    K Number
    K210341
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1155
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Spd Swiss Precision Diagnostics GmbH
    Date Received
    February 5, 2021
    Decision Date
    March 10, 2022
    Product Code
    LCX
    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
    LCX Kit, Test, Pregnancy, Hcg, Over The Counter

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    Other Clearances by Spd Swiss Precision Diagnostics GmbH

    K Number Device Name
    K240025 Clearblue® Early Detection Pregnancy Test
    K213379 Clearblue ® Early Pregnancy Test
    K200913 Clearblue® Early Digital Pregnancy Test