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

    CURITY ANESTHESIA FILTER

    K Number: K864103 · Decision Jan 28, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    141
    Registration Numbers
    141
    Same Product Code
    201
    Applicant Total
    63
    Review Days
    99

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    Basic Information

    Device Name
    CURITY ANESTHESIA FILTER
    K Number
    K864103
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5260
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    The Kendal Co.
    Date Received
    October 21, 1986
    Decision Date
    January 28, 1987
    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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    Other Clearances by The Kendal Co.

    K Number Device Name
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    K991758 MONOJECT INSULIN SYRINGE
    K970969 KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SET
    K951488 KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAP
    K942664 KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM
    K942774 POLYSKIN(R) M.R. MOIST RESPONSIVE TRANSPARENT DRESSING
    K892434 KENDALL CURITY OXYGEN MASK
    K892438 KENDALL CURITY INTRAVASCULAR CUT DOWN TUBES
    K892440 KENDALL CURITY EXTENSION TUBES
    Search all 63 clearances from The Kendal Co. →