Surgical Laser Technologies, Inc.
MODIFICATION TO: LASERPRO 810, 940, AND 980 DIODE DIODE LASER SYSTEMS
SKU K042211UPC GEX
In Stock
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IIFDA 510(k) Cleared (K042211)
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Free shipping on orders over $99 · 30-day returns
Surgical Laser Technologies, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO: LASERPRO 810, 940, AND 980 DIODE DIODE LASER SYSTEMS is an FDA 510(k)-cleared medical device (K042211) manufactured by Surgical Laser Technologies, 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 November 7, 2004. Regulation: 8.
