Electro-Diagnostic Imaging, Inc.
MODIFICATION TO EDI VERIS SYSTEM
SKU K003442UPC HLX
In Stock
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IIFDA 510(k) Cleared (K003442)
1
Free shipping on orders over $99 · 30-day returns
Electro-Diagnostic Imaging, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO EDI VERIS SYSTEM is an FDA 510(k)-cleared medical device (K003442) manufactured by Electro-Diagnostic Imaging, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 3, 2001. Regulation: 8.
