BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

    ONE STEP SINGLE/MULTI-DRUG TEST CUP, ONE STEP SINGLE/MULTI-DRUG TEST DIPCARD

    K Number: K140748 · Decision Aug 20, 2014
    View on FDA
    Classifications
    1
    FEI Numbers
    100
    Registration Numbers
    100
    Same Product Code
    214
    Applicant Total
    10
    Review Days
    148

    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
    ONE STEP SINGLE/MULTI-DRUG TEST CUP, ONE STEP SINGLE/MULTI-DRUG TEST DIPCARD
    K Number
    K140748
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.3650
    Medical Specialty
    Clinical Toxicology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Co-Innovation Biotech Co., Ltd.
    Date Received
    March 25, 2014
    Decision Date
    August 20, 2014
    Product Code
    DJG
    Advisory Committee
    Clinical Toxicology
    Review Advisory Committee
    TX
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DJG Enzyme Immunoassay, Opiates

    Similar 510(k) Clearances

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

    Labcorp Fentanyl Urine Visual Test

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Evidence MultiSTAT DOA Urine MultiPlex

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    LZI Buprenorphine II Enzyme Immunoassay

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    SEFRIA™ Hydrocodone Oral Fluid

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Healgen® AccuFluor Fentanyl Fluorescence Immunoassay (FIA)Test Kit - Qualitative; Healgen® Immunofluorescence Analyzer (OG-H180)

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    LZI Fentanyl III Enzyme Immunoassay

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology
    View all

    Other Clearances by Co-Innovation Biotech Co., Ltd.

    K Number Device Name
    K241100 Rapid Urine Fentanyl (FYL) Test Strip; Rapid Urine Fentanyl (FYL) Test Dipcard
    K231904 Rapid Fentanyl (FYL) Test Strip, Rapid Fentanyl (FYL) Test Dipcard
    K232732 Rapid Marijuana (THC) Test Strip 20, Rapid Marijuana (THC) Test Dipcard 20, Rapid Marijuana (THC) Test Strip 50, Rapid Marijuana (THC) Test Dipcard 50
    K213808 Co-Innovation One Step Human Chorionic Gonadotropin (HCG) Test Strip, Co-Innovation One Step Human Chorionic Gonadotropin (HCG) Test Cassette, Co-Innovation One Step Human Chorionic Gonadotropin (HCG) Test Midstream
    K153050 Rapid Single/Multi-drug Test Cup, Rapid Single/Multi-drug Test Dipcard
    K142800 Rapid Single/Multi-drug Test Cup and Rapid Single/Multi-drug Test Dipcard
    K140215 ONE STEP SINGLE/MULTI-DRUG TEST CUP/DIPCARD
    K131110 ONE STEP SINGLE/MULTI-DRUG TEST CUP; ONE STEP SINGLE SINGLE/MULTI-DRUG TEST DIPCARD
    K132085 ONE STEP HCG TEST STRIP, ONE STEP HCG TEST CASSETTE, ONE STEP HCG TEST MIDSTREAM