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

    DISPOSABLE O.R. TOWEL, STERILE

    K Number: K915740 · Decision Jun 22, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    200
    Registration Numbers
    200
    Same Product Code
    449
    Applicant Total
    20
    Review Days
    182

    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
    DISPOSABLE O.R. TOWEL, STERILE
    K Number
    K915740
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4370
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    American Threshold Industries, Inc.
    Date Received
    December 23, 1991
    Decision Date
    June 22, 1992
    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

    Similar 510(k) Clearances

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

    BeneHold™ Surgical Incise Drape with CHG antimicrobial II

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    3M™ Ioban™ CHG Chlorhexidine Gluconate Incise Drape (contains 2% w/w CHG)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BeneHold Surgical Incise Drape with CHG antimicrobial

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ControlRad Sterile Cover

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MediClear PreOp

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Plus Surgical Drapes (EO Sterilized), PMDB-XXX

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery
    View all

    Other Clearances by American Threshold Industries, Inc.

    K Number Device Name
    K971483 SECURE-WRAP (TM) STERILIZATION WRAP
    K953879 SURGEON'S CAP
    K953878 BOUFFANT CAP
    K952114 KOOL GARD SINGLES GOWN
    K952115 BARRIER GOWN, KOOL-GARD BACKLESS GOWN
    K952116 COVER GOWN
    K934085 MODIFICATION OF SURGICAL EYESHIELD MASK
    K915530 NOVA GAUZE(R) DISPOSABLE NONWOVEN SPONGES, STERILE
    K912110 DISPOSABLE O.R. TOWEL
    K894383 DISPOSABLE SHOE COVER
    Search all 20 clearances from American Threshold Industries, Inc. →