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    Patient Details Specimen Details Physician Details

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    Max Wells
    The document is a patient report from a lab showing results for a SARS-CoV-2 test. The test for the patient, Sylvia Ramos, was detected as positive. Additional information is provided about the test and notes about collection date.

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    © All Rights Reserved
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    Patient Details Specimen Details Physician Details

    Uploaded by

    Max Wells
    320 views1 page
    The document is a patient report from a lab showing results for a SARS-CoV-2 test. The test for the patient, Sylvia Ramos, was detected as positive. Additional information is provided about the test and notes about collection date.

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    Djdkje

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    Copy of 6

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    The document is a patient report from a lab showing results for a SARS-CoV-2 test. The test for the patient, Sylvia Ramos, was detected as positive. Additional information is provided about the test and notes about collection date.

    Copyright:

    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Download as pdf or txt
    320 views1 page

    Patient Details Specimen Details Physician Details

    Uploaded by

    Max Wells
    The document is a patient report from a lab showing results for a SARS-CoV-2 test. The test for the patient, Sylvia Ramos, was detected as positive. Additional information is provided about the test and notes about collection date.

    Copyright:

    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Download as pdf or txt
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    1 Patient Report 

      
    Specimen ID: 148-229-6453-0 Acct #: 04115970 Phone: (909) 677-7168 Rte: 00
    Control ID: PRP04115970
    SBDPH_WH
    RAMOS SYLVIA 247 S BOYD STREET
    10796 PEMBERTON ST SAN BERNARDINO CA 92415
    

    ADELANTO , CA 92301
    (909) 496-1977

    Patient Details Specimen Details Physician Details


    DOB: 09/16/1978 Date collected: 06/22/2020 1230 Ordering: E GUSTAFSON
    Age(y/m/d): 041/08/16 Date received: 06/23/2020 Referring:
    Gender: F Date entered: 06/23/2020 ID:
    Patient ID: Date reported: 06/25/2020 2005 ET NPI: 1770877060
    Ordered Items
    SARS-CoV-2, NAA; Please note
    TESTS RESULT FLAG UNITS REFERENCE INTERVAL LAB
    SARS-CoV-2, NAA Detected Critical Not Detected 01
    This test was developed and its performance characteristics determined
    by LabCorp Laboratories. This test has not been FDA cleared or
    approved. This test has been authorized by FDA under an Emergency Use
    Authorization (EUA). This test is only authorized for the duration of
    time the declaration that circumstances exist justifying the
    authorization of the emergency use of in vitro diagnostic tests for
    detection of SARS-CoV-2 virus and/or diagnosis of COVID-19 infection
    under section 564(b)(1) of the Act, 21 U.S.C. 360bbb-3(b)(1), unless
    the authorization is terminated or revoked sooner.
    When diagnostic testing is negative, the possibility of a false
    negative result should be considered in the context of a patient's
    recent exposures and the presence of clinical signs and symptoms
    consistent with COVID-19. An individual without symptoms of COVID-19
    and who is not shedding SARS-CoV-2 virus would expect to have a
    negative (not detected) result in this assay.

    Please note 02
    The date and/or time of collection was not indicated on the
    requisition as required by state and federal law. The date of
    receipt of the specimen was used as the collection date if not
    supplied.

    01 CETWE LabCorp Phoenix Dir: Earle Collum, MD


    5005 S 40th St, Phoenix, AZ 85040-2969
    02 SO LabCorp San Diego Dir: Jenny Galloway, MD
    13112 Evening Creek Dr So Ste 200, San Diego, CA
    92128-4108
    For inquiries, the physician may contact Branch: 800-859-6046 Lab: 800-788-9743

    Date Issued: 06/25/2020 211 ET FINAL REPORT Page 1 of 1


    This document contains private and confidential health information protected by state and federal law. © 1995-2020 Laboratory Corporation of America® Holdings
    If you have received this document in error, please call 858-668-3700 1.00
    All Rights Reserved - Enterprise Report Version:          

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