ULTIMA FIVE— 510(k) K083494

Substantially Equivalent

Pain Management Technologies

FDA 510(k) clearance K083494 for ULTIMA FIVE, Substantially Equivalent on 2009-01-06. Applicant: Pain Management Technologies. Device class: 2.

Clearance details

Applicant: Pain Management Technologies
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2008-11-25
Decision date: 2009-01-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Akron, OH, 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.