TENS/IF 14— 510(k) K071869

Substantially Equivalent

Emsi

FDA 510(k) clearance K071869 for TENS/IF 14, Substantially Equivalent on 2008-03-07. Applicant: Emsi. Device class: 2.

Clearance details

Applicant: Emsi
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2007-07-06
Decision date: 2008-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alexandria, VA, 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.