ACTIVATOR V-E— 510(k) K112606

Name: FDA 510(k) clearance K112606
Creator: U.S. Food and Drug Administration
Published: 2012-03-06

Substantially Equivalent

Activator Methods International, Ltd.

FDA 510(k) clearance K112606 for ACTIVATOR V-E, Substantially Equivalent on 2012-03-06. Applicant: Activator Methods International, Ltd.. Device class: Unclassified.

Clearance details

Applicant: Activator Methods International, Ltd.
Product code: Code LXM
Device class: Unclassified
Advisory panel: Unknown
Date received: 2011-09-08
Decision date: 2012-03-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Phoenix, AZ, US

Download summary PDF View on FDA.gov ↗

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