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

    RESPIRATORY KIT

    K Number: K772047 · Decision Nov 23, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    141
    Registration Numbers
    141
    Same Product Code
    201
    Applicant Total
    56
    Review Days
    26

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    Basic Information

    Device Name
    RESPIRATORY KIT
    K Number
    K772047
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5260
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    American Hospital Supply Corp.
    Date Received
    October 28, 1977
    Decision Date
    November 23, 1977
    Product Code
    CAH
    Advisory Committee
    Anesthesiology
    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
    CAH Filter, Bacterial, Breathing-Circuit

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    K830343 CONTAINER W/PRIMING SOLUTION
    K830301 STRATUS FLUOROMETRIC ENZYME IMMUN0-
    K822755 LATEX PENROSE TUBING
    K823418 HEYER-SCHUTE UNIVERSAL URETERAL STENT
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