510(k) K231137

Device
Xenta Drug Screen Cup, Xenta Drug Screen Dipcard
Applicant
Xenta Biomedical Science Co., Ltd.
510(k) number
K231137
Product code
DKZ
Decision
Substantially Equivalent (SESE)
Decision date
2023-05-19
Date received
2023-04-21
Regulation
862.3100
Classification name
Enzyme Immunoassay, Amphetamine
Medical specialty
Clinical Toxicology
Review panel
Clinical Toxicology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Huang Ling
Address
Bldg. C5, 9th Floor, Rm.901, # 11 Kaiyuan Ave., Huangpu District Guangzhou CN 510535 510535

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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510(k), Device, Applicant table
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