QUICKSCREEN PRO MULTI DRUG SCREEN, MODEL 9177 & 9178— 510(k) K993165

Name: FDA 510(k) clearance K993165
Creator: U.S. Food and Drug Administration
Published: 1999-10-20

Substantially Equivalent

Phamatech

FDA 510(k) clearance K993165 for QUICKSCREEN PRO MULTI DRUG SCREEN, MODEL 9177 & 9178, Substantially Equivalent on 1999-10-20. Applicant: Phamatech. Device class: 2.

Clearance details

Applicant: Phamatech
Product code: Code DJG
Device class: Class 2
Regulation: 21 CFR 862.3650
Advisory panel: Clinical Toxicology
Date received: 1999-09-22
Decision date: 1999-10-20
Decision: Substantially Equivalent
Clearance type: Special
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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