ELECTROPULSE— 510(k) K051128

Substantially Equivalent

Pain Relief Technologies

FDA 510(k) clearance K051128 for ELECTROPULSE, Substantially Equivalent on 2006-03-10. Applicant: Pain Relief Technologies. Device class: 2.

Clearance details

Applicant: Pain Relief Technologies
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2005-05-03
Decision date: 2006-03-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Scottsdale, AZ, 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.