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

    CATH-FINDER

    K Number: K931073 · Decision May 5, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    204
    Registration Numbers
    205
    Same Product Code
    503
    Applicant Total
    43
    Review Days
    429

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    Basic Information

    Device Name
    CATH-FINDER
    K Number
    K931073
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5200
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Pharmacia Deltec, Inc.
    Date Received
    March 2, 1993
    Decision Date
    May 5, 1994
    Product Code
    FOZ
    Advisory Committee
    General Hospital
    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
    FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

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    Other Clearances by Pharmacia Deltec, Inc.

    K Number Device Name
    K943310 MODEL 6100 AMBULATORY INFUSION SYSTEM
    K942046 PHARMACIA DELTEC EXTENSION SET WITH ANTI-SIPHON VALVE
    K942161 LOCKBOX
    K942024 PORT-A-CATH LOW PROFILE IMPLANTABLE VENOUS ACCESS SYSTEM
    K941445 EXTENSION SET WITH ANTI-SIPHON VALVE
    K932430 DUAL LUMEN PERIPHERALLY INSERTED VENOUS CATHETER
    K932433 PHERIPHERALLY INSERTED VENOUS CATHETER-Y SITE
    K932198 PHARMACIA DELTEC PERIPHERALLY INSERTED VENOUS CATH
    K932464 PERIPHERALLYINSRTED VENOUS CATH. ALTERNATE CATH.
    K932211 PROCEDURAL TRAY FOR PERIPHERALLY INSERTED VENOUS
    Search all 43 clearances from Pharmacia Deltec, Inc. →