Aurora Imaging Technology, Inc.
AURORA MAGNETIC RESONANCE DIAGNOSTIC DEVICE
SKU K012154UPC LNH
In Stock
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IIFDA 510(k) Cleared (K012154)
1
Free shipping on orders over $99 · 30-day returns
Aurora Imaging Technology, Inc.
Free shipping on orders over $99 · 30-day returns
AURORA MAGNETIC RESONANCE DIAGNOSTIC DEVICE is an FDA 510(k)-cleared medical device (K012154) manufactured by Aurora Imaging Technology, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 18, 2001. Regulation: 8.
