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

    ACE CEDIA PHENOBARBITAL ASSAY

    K Number: K942501 · Decision Oct 6, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    25
    Registration Numbers
    25
    Same Product Code
    34
    Applicant Total
    24
    Review Days
    135

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    Basic Information

    Device Name
    ACE CEDIA PHENOBARBITAL ASSAY
    K Number
    K942501
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.3660
    Medical Specialty
    Clinical Toxicology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Schiapparelli Biosystems, Inc.
    Date Received
    May 24, 1994
    Decision Date
    October 6, 1994
    Product Code
    DLZ
    Advisory Committee
    Clinical Toxicology
    Review Advisory Committee
    CH
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    DLZ Enzyme Immunoassay, Phenobarbital

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    Other Clearances by Schiapparelli Biosystems, Inc.

    K Number Device Name
    K991733 ACE LDL-C REAGENT, LDL-C CALIBRATOR, LDL-C CONTROLS
    K981377 ACE T4 REAGENT T4 CALIBRATORS
    K981375 ACE T UPTAKE REAGENT TU CALIBRATORS
    K973581 ACE VALPROIC ACID REAGENT, AED CALIBRATORS
    K973583 ACE THEOPHYLLINE REAGENT, THEO CALIBRATORS
    K973582 ACE PRIMIDONE REAGENT, AED CALIBRATORS
    K973536 ACE PHENOBARBITAL REAGENT/AED CALIBRATORS
    K973414 ACE PHENYTOIN REAGENT, AED CALIBRATORS
    K973535 ACE CARBAMAZEPINE REAGENT/AED CALIBRATORS
    K971526 ACE HDL-C REAGENT
    Search all 24 clearances from Schiapparelli Biosystems, Inc. →