Intra Lase Corp.
INTRALASE FS LASER
SKU K041893UPC GEX
In Stock
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IIFDA 510(k) Cleared (K041893)
1
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Intra Lase Corp.
Free shipping on orders over $99 · 30-day returns
INTRALASE FS LASER is an FDA 510(k)-cleared medical device (K041893) manufactured by Intra Lase Corp.. 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 July 28, 2005. Regulation: 8.
