Lumenis, Inc.
MODIFIED VERSAPULSE SELECT HO:YAG AND HO:YAG/ND:YAG LASERS
SKU K980685UPC GEX
In Stock
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IIFDA 510(k) Cleared (K980685)
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Free shipping on orders over $99 · 30-day returns
Lumenis, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFIED VERSAPULSE SELECT HO:YAG AND HO:YAG/ND:YAG LASERS is an FDA 510(k)-cleared medical device (K980685) 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 May 19, 1998. Regulation: 8.
