ACTIVAPATCH— 510(k) K091326

Substantially Equivalent

Activatek, Inc.

FDA 510(k) clearance K091326 for ACTIVAPATCH, Substantially Equivalent on 2009-05-27. Applicant: Activatek, Inc.. Device class: 2.

Clearance details

Applicant: Activatek, Inc.
Product code: Code EGJ
Device class: Class 2
Regulation: 21 CFR 890.5525
Advisory panel: Physical Medicine
Date received: 2009-05-05
Decision date: 2009-05-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Valley, UT, US

Download summary PDF View on FDA.gov ↗

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