EMPI ACTIVE TRANSCUTANEOUS NERVE STIMULATOR— 510(k) K090922

Name: FDA 510(k) clearance K090922
Creator: U.S. Food and Drug Administration
Published: 2009-06-05

Substantially Equivalent

Empi

FDA 510(k) clearance K090922 for EMPI ACTIVE TRANSCUTANEOUS NERVE STIMULATOR, Substantially Equivalent on 2009-06-05. Applicant: Empi. Device class: 2.

Clearance details

Applicant: Empi
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2009-04-01
Decision date: 2009-06-05
Decision: Substantially Equivalent
Clearance type: Special
Location: Clear Lake, SD, 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.