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

    PN 62290 0.22 MICRON MICRO INFUS I.V. EXTEN SET

    K Number: K914792 · Decision Jan 15, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    424
    Registration Numbers
    424
    Same Product Code
    1173
    Applicant Total
    10
    Review Days
    84

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    PN 62290 0.22 MICRON MICRO INFUS I.V. EXTEN SET
    K Number
    K914792
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5440
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Filtertek, Inc.
    Date Received
    October 23, 1991
    Decision Date
    January 15, 1992
    Product Code
    FPA
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FPA Set, Administration, Intravascular

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (FPA), ordered by most recent decision date.

    iiSure Infusion Set

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PuraCath Firefly Needleless Connector IT (9005)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD Alaris Pump Infusion Set

    FDA 510(k)
    FDA Class 2 ·General Hospital

    EZ™ IV Administration Set

    FDA 510(k)
    FDA Class 2 ·General Hospital
    View all

    Other Clearances by Filtertek, Inc.

    K Number Device Name
    K981548 NFC NEEDLEFREE CONNECTOR MODEL 69900
    K981547 NFC NEEDLEFREE Y-SITE, MODEL 69970
    K912848 I.V. FILTER EXTENSION SET
    K912394 TRANSDUCER PROTECTOR
    K911451 I.V. EXTENDER SET
    K904912 TRANSDUCER PROTECTOR
    K901409 TRANSDUCER PROTECTOR
    K901996 FILTERTEK PN 60650 DIALYSIS TRANSDUCER PROTECTOR
    K895281 TRANSDUCER PROTECTOR