Neuro Resource Group, Inc.
INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE
SKU K070217UPC NFO
In Stock
—
IIFDA 510(k) Cleared (K070217)
1
Free shipping on orders over $99 · 30-day returns
Healix Assistant
Ask me anything about our products
Quick questions
Powered by Healix AI · Talk to a human
Neuro Resource Group, Inc.
Free shipping on orders over $99 · 30-day returns
INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE is an FDA 510(k)-cleared medical device (K070217) manufactured by Neuro Resource Group, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 3, 2008. Regulation: 8.
