Konica Minolta Medical & Graphic, Inc.
LASER IMAGER DRYPRO MODEL 873
SKU K081637UPC LMC
In Stock
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IIFDA 510(k) Cleared (K081637)
1
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Konica Minolta Medical & Graphic, Inc.
Free shipping on orders over $99 · 30-day returns
LASER IMAGER DRYPRO MODEL 873 is an FDA 510(k)-cleared medical device (K081637) 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 June 30, 2008. Regulation: 8.
