ELECTROPULSE - LOW BACK PAIN— 510(k) K062532

Substantially Equivalent

Pain Relief Technologies

FDA 510(k) clearance K062532 for ELECTROPULSE - LOW BACK PAIN, Substantially Equivalent on 2007-02-09. Applicant: Pain Relief Technologies.

Clearance details

Applicant: Pain Relief Technologies
Product code: Code NUH
Advisory panel: Neurology
Date received: 2006-08-28
Decision date: 2007-02-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Beaverton, OR, US

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