Nidek, Inc.
DIO-LIGHT LASER SYSTEM
SKU K980201UPC GEX
In Stock
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IIFDA 510(k) Cleared (K980201)
1
Free shipping on orders over $99 · 30-day returns
Nidek, Inc.
Free shipping on orders over $99 · 30-day returns
DIO-LIGHT LASER SYSTEM is an FDA 510(k)-cleared medical device (K980201) manufactured by Nidek, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 15, 1998. Regulation: 8.
