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

    CEREGLIDE 92 Catheter System

    K Number: K233982 · Decision May 9, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    72
    Registration Numbers
    72
    Same Product Code
    91
    Applicant Total
    8
    Review Days
    143

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    Basic Information

    Device Name
    CEREGLIDE 92 Catheter System
    K Number
    K233982
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    870.1250
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Cerenovus, Inc.
    Date Received
    December 18, 2023
    Decision Date
    May 9, 2024
    Product Code
    QJP
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    QJP Catheter, Percutaneous, Neurovasculature

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    Other Clearances by Cerenovus, Inc.

    K Number Device Name
    K251828 CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set
    K241221 CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing Set
    K241244 CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter
    K233988 Cerenovus Large Bore Catheter; Cerenovus Aspiration Tubing Set
    K230726 CEREGLIDE 92 Intermediate Catheter
    K221930 CEREGLIDE 71 Intermediate Catheter
    K221934 CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set