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

    091 Balloon Guide Catheter

    K Number: K220331 · Decision Jul 29, 2022
    View on FDA
    Classifications
    1
    FEI Numbers
    276
    Registration Numbers
    277
    Same Product Code
    889
    Applicant Total
    9
    Review Days
    175

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    Basic Information

    Device Name
    091 Balloon Guide Catheter
    K Number
    K220331
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1250
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Inneuroco, Inc.
    Date Received
    February 4, 2022
    Decision Date
    July 29, 2022
    Product Code
    DQY
    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
    DQY Catheter, Percutaneous

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    Other Clearances by Inneuroco, Inc.

    K Number Device Name
    K232260 Thinline Sheath Introducer
    K190338 046 Zenith Flex
    K181354 074 Zenith Flex System
    K172167 Zenith Flex System
    K173709 Zenith Support, 95 cm, Zenith Support, 105 cm, Zenith Support, 115 cm
    K172468 091 Long Sheath, 70 cm, 091 Long Sheath, 80 cm, 091 Long Sheath, 90 cm
    K171672 065 Zenith, 074 Zenith
    K161262 Super Distal Access (SDA)