NEUROMED ELECTROANALGESIC DELIVERY SYSTEMS— 510(k) K083250

Name: FDA 510(k) clearance K083250
Creator: U.S. Food and Drug Administration
Published: 2009-08-18

Substantially Equivalent

Aa Neuromed Corp.

FDA 510(k) clearance K083250 for NEUROMED ELECTROANALGESIC DELIVERY SYSTEMS, Substantially Equivalent on 2009-08-18. Applicant: Aa Neuromed Corp.. Device class: 2.

Clearance details

Applicant: Aa Neuromed Corp.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2008-11-04
Decision date: 2009-08-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Port Coquitlam, Bc, CA

Download summary PDF View on FDA.gov ↗

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