Microlight Corporation of America
MICROLIGHT 830 LASER SYSTEM
SKU K010175UPC NHN
In Stock
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IIFDA 510(k) Cleared (K010175)
1
Free shipping on orders over $99 · 30-day returns
Microlight Corporation of America
Free shipping on orders over $99 · 30-day returns
MICROLIGHT 830 LASER SYSTEM is an FDA 510(k)-cleared medical device (K010175) manufactured by Microlight Corporation of America. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 5, 2002. Regulation: 8.
