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

    DYNAJECT

    K Number: K790835 · Decision Jun 22, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    124
    Registration Numbers
    124
    Same Product Code
    209
    Applicant Total
    10
    Review Days
    53

    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
    DYNAJECT
    K Number
    K790835
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1650
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Atomic Products Corp.
    Date Received
    April 30, 1979
    Decision Date
    June 22, 1979
    Product Code
    DXT
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DXT Injector And Syringe, Angiographic

    Similar 510(k) Clearances

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

    Disposable Syringes with Accessories for Power Injectors (900103T); Disposable Syringes with Accessories for Power Injectors (900103H); Disposable Syringes with Accessories for Power Injectors (801800H); Disposable Syringes with Accessories for Power Injectors (800099T); Disposable Syringes with Accessories for Power Injectors (800099H); Disposable Syringes with Accessories for Power Injectors (800096T); Disposable Syringes with Accessories for Power Injectors (800096H); Disposable Syr

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACIST Pro Diagnostic System (019304); Processing Unit Bed Mount; AngioTouch Module; ACIST Pro Cart; Single Transducer Cable; Triple Transducer Cable

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VeraPro S100 Multi-Use Syringe (018808); VeraPro S100 LV1 Low Viscosity Single-Use Syringe (018811); VeraPro AMT Auto-Manifold and Transducer (018814); VeraPro AngioTouch FLX165 Hand Controller Kit (018806); VeraPro AngioTouch HiFi165 Hand Controller Kit (018804)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    High Pressure Syringe; Pressure Connecting Tube; Quick fill tube; Spike; Transfer Tube

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Extension tube

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDRAD MRXperion MR Injection System and MR Injection System Syringe Kit; MEDRAD ISI2 Module (ISI2)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular
    View all

    Other Clearances by Atomic Products Corp.

    K Number Device Name
    K915541 SPECT TABLE, MODEL #056-760
    K913055 THYROID UPTAKE SYST/AUTOMLAB 900 MEDI SPEC 187-900
    K904187 ECONOMY C-ARM TABLE, MODEL # 056-005
    K904623 RADIOGRAPHIC TRANSPORT, TRAUMA MODEL 056-230, 235
    K900851 DIGITAL IMAGE ENHANCEMENT SYSTEM
    K895799 RECTILINEAR SCANNER MODEL #187-270
    K884312 ATOMLAB 100, MODEL 086-250 & 200 MODEL 086-270
    K871868 VENTI-SCAN II
    K874332 MRI STRETCHER