BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    ADT MINI PERITONEAL LAVAGE KIT

    K Number: K800422 · Decision Mar 12, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    57
    Registration Numbers
    57
    Same Product Code
    16
    Applicant Total
    21
    Review Days
    15

    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
    ADT MINI PERITONEAL LAVAGE KIT
    K Number
    K800422
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4200
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    A.D.T. Lab Industries
    Date Received
    February 26, 1980
    Decision Date
    March 12, 1980
    Product Code
    GBW
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GBW Catheter, Peritoneal

    Similar 510(k) Clearances

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

    MINI-PORT

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    INTRADUCER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    INTRADUCER PORT SC CATALOG#31275,31035,30915, AND 31450

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ANTIMICROBIAL MEDIASTINAL SILICONE DRAIN

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    MEDICOMP FLEXI-SMOOTH WOUND DRAINAGE CATHETER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    MEDIASTINAL SILICONE DRAINS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery
    View all

    Other Clearances by A.D.T. Lab Industries

    K Number Device Name
    K812297 A.D.T. PROCEDURES TRAY
    K801754 ADT BONE MARROW ASPIRATION NEEDLE
    K801753 ADT BONE MARROW BIOPSY-ASPIR. NEELDE
    K800410 ADT BONE MARROW BIOPSY-ASPIRATION TRAY
    K800417 ADT PTC PRO. TRAY W/(SKINNY CHIBA) NEEDL
    K800411 ASPIRATION TRAY W/FERRIS DISP. ILLINOIS
    K800418 ADT DISPOSABLE THIN NEEDLE ASPIRATION
    K800414 ADT SOFT TISSUE BIOPSY TRAY
    K800408 ADT BONE MAR. BIO/ASP. TRAY W/NEEDLE
    K800409 ADT BONE MARROW BIOPSY ASPIRATION TRAY
    Search all 21 clearances from A.D.T. Lab Industries →