Intra Lase Corp.
INTRALASE FS LASER, INTRALASE FS30 LASER, MODELS 1, 2, 3
SKU K060372UPC GEX
In Stock
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IIFDA 510(k) Cleared (K060372)
1
Free shipping on orders over $99 · 30-day returns
Intra Lase Corp.
Free shipping on orders over $99 · 30-day returns
INTRALASE FS LASER, INTRALASE FS30 LASER, MODELS 1, 2, 3 is an FDA 510(k)-cleared medical device (K060372) 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 August 15, 2006. Regulation: 8.
