INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE— 510(k) K070217

Substantially Equivalent

Neuro Resource Group, Inc.

FDA 510(k) clearance K070217 for INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE, Substantially Equivalent on 2008-04-04. Applicant: Neuro Resource Group, Inc..

Clearance details

Applicant: Neuro Resource Group, Inc.
Product code: Code NFO
Advisory panel: Neurology
Date received: 2007-01-23
Decision date: 2008-04-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Plano, TX, US

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