JOINT STIM, MODEL 1000— 510(k) K073386

Name: FDA 510(k) clearance K073386
Creator: U.S. Food and Drug Administration
Published: 2008-07-30

Substantially Equivalent

Pain Management Technologies

FDA 510(k) clearance K073386 for JOINT STIM, MODEL 1000, Substantially Equivalent on 2008-07-30. Applicant: Pain Management Technologies. Device class: 2.

Clearance details

Applicant: Pain Management Technologies
Product code: Code NYN
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2007-12-03
Decision date: 2008-07-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Akron, OH, US

Download summary PDF View on FDA.gov ↗

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