Lumenis, Inc.
VERSAPULSE MODEL P20 LASER SYSTEM
SKU K100228UPC GEX
In Stock
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IIFDA 510(k) Cleared (K100228)
1
Free shipping on orders over $99 · 30-day returns
Lumenis, Inc.
Free shipping on orders over $99 · 30-day returns
VERSAPULSE MODEL P20 LASER SYSTEM is an FDA 510(k)-cleared medical device (K100228) manufactured by Lumenis, 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 February 23, 2010. Regulation: 8.
