Lasermatic, Inc.
MODIFIED COMBOLASER 5050 & NEW MODEL 5050 VER. 33
SKU K901638UPC GEX
In Stock
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IIFDA 510(k) Cleared (K901638)
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Free shipping on orders over $99 · 30-day returns
Lasermatic, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFIED COMBOLASER 5050 & NEW MODEL 5050 VER. 33 is an FDA 510(k)-cleared medical device (K901638) manufactured by Lasermatic, 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 June 26, 1990. Regulation: 8.
