Lunar Corp.
LUNAR REPORT GENERATOR II
SKU K001756UPC KGI
In Stock
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IIFDA 510(k) Cleared (K001756)
1
Free shipping on orders over $99 · 30-day returns
Lunar Corp.
Free shipping on orders over $99 · 30-day returns
LUNAR REPORT GENERATOR II is an FDA 510(k)-cleared medical device (K001756) manufactured by Lunar Corp.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 5, 2000. Regulation: 8.
