Mdi, Inc.
LASEAWAY Q-SWITCHED ND:YAG LASER SYSTEM
SKU K942622UPC GEX
In Stock
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IIFDA 510(k) Cleared (K942622)
1
Free shipping on orders over $99 · 30-day returns
Mdi, Inc.
Free shipping on orders over $99 · 30-day returns
LASEAWAY Q-SWITCHED ND:YAG LASER SYSTEM is an FDA 510(k)-cleared medical device (K942622) manufactured by Mdi, 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 23, 1995. Regulation: 8.
