ACTIVAPATCH ET IONTOPHORESIS PATCH— 510(k) K132832

Name: FDA 510(k) clearance K132832
Creator: U.S. Food and Drug Administration
Published: 2014-02-13

Substantially Equivalent

Activatek, Inc.

FDA 510(k) clearance K132832 for ACTIVAPATCH ET IONTOPHORESIS PATCH, Substantially Equivalent on 2014-02-13. 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: 2013-09-10
Decision date: 2014-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Valley City, 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.