AIRISTAR AIR PURIFICATION SYSTEM, MODEL 500 & 1000— 510(k) K072185

Name: FDA 510(k) clearance K072185
Creator: U.S. Food and Drug Administration
Published: 2008-03-27

Substantially Equivalent

Airistar Technologies, LLC

FDA 510(k) clearance K072185 for AIRISTAR AIR PURIFICATION SYSTEM, MODEL 500 & 1000, Substantially Equivalent on 2008-03-27. Applicant: Airistar Technologies, LLC. Device class: 2.

Clearance details

Applicant: Airistar Technologies, LLC
Product code: Code FRF
Device class: Class 2
Regulation: 21 CFR 880.5045
Advisory panel: General Hospital
Date received: 2007-08-06
Decision date: 2008-03-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deer Field, IL, US

Download summary PDF View on FDA.gov ↗

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