QUICKSCREEN AMPHETINE 500 TEST— 510(k) K131069

Substantially Equivalent

Phamatech, Inc.

FDA 510(k) clearance K131069 for QUICKSCREEN AMPHETINE 500 TEST, Substantially Equivalent on 2014-05-14. Applicant: Phamatech, Inc..

Clearance details

Applicant: Phamatech, Inc.
Product code: Code DKZ
Advisory panel: Clinical Toxicology
Date received: 2013-04-17
Decision date: 2014-05-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.