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

    FLUID REMOVAL ASSEMBLY

    K Number: K840490 · Decision Apr 17, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    548
    Registration Numbers
    548
    Same Product Code
    747
    Applicant Total
    42
    Review Days
    71

    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
    FLUID REMOVAL ASSEMBLY
    K Number
    K840490
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5860
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Ackrad Laboratories
    Date Received
    February 6, 1984
    Decision Date
    April 17, 1984
    Product Code
    FMF
    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
    FMF Syringe, Piston

    Similar 510(k) Clearances

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

    Sol-Glide Safety Needle; Sol-Glide Safety Needle with Syringe

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Profoject™ Safety Needle; Profoject™ Syringe with Safety Needle; Profoject™ Low Dead Space Syringe with Safety Needle

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Sofjec (Single use Needle); Sofjec (Single use Syringe with or without Needle); Sofjec (Membrane Filter Syringe)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Sterile Hypodermic Syringe for Single Use (20ml, 30ml, 50ml, 60ml)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Profoject™ Insulin Syringes; Profoject™ Safelock Disposable Insulin Syringe

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Instylla Delivery Kit

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

    Other Clearances by Ackrad Laboratories

    K Number Device Name
    K021272 SIB CATHETER, MODEL 61-7005
    K020954 H/S PROCEDURE TRAY (5F), H/S PROCEDURE TRAY (7F), H/S ELLIPTOSPHERE PROCEDURE TRAY & MULTIPURPOSE PROCEDURE TRAY
    K020951 H/S CATHETER SET (5F), MODEL 61-5005; H/S CATHETER SET (7F), MODEL 61-5007
    K970492 INTRAUTERINE INSEMINATION AND SONOHYSTEROGRAPHY CATHETER
    K961752 H/S CATHETER SET(61-3005, 61-3007, 61-3605, 61-3607)
    K940176 ACKRAD IUI SET FOR INTRAUTERINE INSEMINATION
    K952542 ACKRAD ESOPHAGEAL BALLOON CATHETER SET
    K953034 H/S CATHETER SET(61-3005, 61-3007, 61-3605, 61-3607)
    K915813 ACKRAD ERCP CONTRAST DELIVERY SET
    K904499 NICOS (NON-INVASIVE CARDIAC OUTPUT SYSTEM)
    Search all 42 clearances from Ackrad Laboratories →