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

    CHEST FLUID MONITOR

    K Number: K772092 · Decision Nov 18, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    69
    Registration Numbers
    69
    Same Product Code
    113
    Applicant Total
    2
    Review Days
    11

    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
    CHEST FLUID MONITOR
    K Number
    K772092
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2770
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Dynatech Research & Development Co.
    Date Received
    November 7, 1977
    Decision Date
    November 18, 1977
    Product Code
    DSB
    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
    DSB Plethysmograph, Impedance

    Similar 510(k) Clearances

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

    BCM2-Body Composition Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Re:Balans

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Edema Guard Monitor (EGM) CardioSet-001

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SOZO Pro

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Zynex Monitoring System, Model CM-1600

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Bodyport Cardiac Scale

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

    Other Clearances by Dynatech Research & Development Co.

    K Number Device Name
    K772093 IMPEDANCE RHEOGRAPH