QUICKSCREEN OXYCODONE TEST, MODELS 9120, 9120T, 9120X AND 9121— 510(k) K043051

Substantially Equivalent

Phamatech, Inc.

FDA 510(k) clearance K043051 for QUICKSCREEN OXYCODONE TEST, MODELS 9120, 9120T, 9120X AND 9121, Substantially Equivalent on 2005-02-07. Applicant: Phamatech, Inc..

Clearance details

Applicant: Phamatech, Inc.
Product code: Code DJG
Advisory panel: Clinical Toxicology
Date received: 2004-11-04
Decision date: 2005-02-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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