Alcon Laboratories, Inc.
WaveLight FS200 Patient Interface
SKU K190392UPC GEX
In Stock
—
IIFDA 510(k) Cleared (K190392)
1
Free shipping on orders over $99 · 30-day returns
Alcon Laboratories, Inc.
Free shipping on orders over $99 · 30-day returns
WaveLight FS200 Patient Interface is an FDA 510(k)-cleared medical device (K190392) manufactured by Alcon Laboratories, 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 25, 2019. Regulation: 8.
