Konica Minolta Medical & Graphic, Inc.
DIRECT DIGITIZER, REGIUS MODEL 110
SKU K071181UPC MQB
In Stock
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IIFDA 510(k) Cleared (K071181)
1
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Konica Minolta Medical & Graphic, Inc.
Free shipping on orders over $99 · 30-day returns
DIRECT DIGITIZER, REGIUS MODEL 110 is an FDA 510(k)-cleared medical device (K071181) manufactured by Konica Minolta Medical & Graphic, 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 May 29, 2007. Regulation: 8.
