ATTEST Drug Screen Cup, ATTEST Drug Screen Dip Card— 510(k) K182123

Name: FDA 510(k) clearance K182123
Creator: U.S. Food and Drug Administration
Published: 2019-03-29

Substantially Equivalent

Advin Biotech, Inc.

FDA 510(k) clearance K182123 for ATTEST Drug Screen Cup, ATTEST Drug Screen Dip Card, Substantially Equivalent on 2019-03-29. Applicant: Advin Biotech, Inc.. Device class: 2.

Clearance details

Applicant: Advin Biotech, Inc.
Product code: Code DJG
Device class: Class 2
Regulation: 21 CFR 862.3650
Advisory panel: Clinical Toxicology
Date received: 2018-08-06
Decision date: 2019-03-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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