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

    O.R. TOWELS (STERILE)

    K Number: K890709 · Decision Mar 14, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    200
    Registration Numbers
    200
    Same Product Code
    449
    Applicant Total
    26
    Review Days
    29

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    Basic Information

    Device Name
    O.R. TOWELS (STERILE)
    K Number
    K890709
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4370
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Cypress Medical Products, Ltd.
    Date Received
    February 13, 1989
    Decision Date
    March 14, 1989
    Product Code
    KKX
    Advisory Committee
    General, Plastic Surgery
    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
    KKX Drape, Surgical, Antimicrobial

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    Other Clearances by Cypress Medical Products, Ltd.

    K Number Device Name
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    K012282 STERILE POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVE
    K972899 CYPRESS MEDICAL PRODUCTS ANEROID SPHYGMOMANOMETER
    K972849 ISOSAFE EARLOOP PROCEDURE MASK (BLUE, YELLOW)
    K972883 ISOSAFE EARLOOP PROCEDURE MASK (BLUE, YELLOW)
    K952367 CYPRESS MEDICAL PRODUCTS VINYL EXAMINATION GLOVE
    K950254 CYPRESS MEDICAL PRODUCTS STERILE LATEX EXAMINATION GLOVE
    K950092 CYPRESS MEDICAL PRODUCTS CATHETER (INSERTION) TRAY
    K950109 CYPRESS MEDICAL PRODUCTS CATHETER (INSERTION) TRAY/WITH OUT CATHETER
    K945082 CYPRESS MEDICAL PRODUCTS STETHOSCOPE
    Search all 26 clearances from Cypress Medical Products, Ltd. →