Buckman Co., Inc.
INCISOR I PULSED ND:YAG LASER SYSTEM
SKU K922901UPC GEX
In Stock
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IIFDA 510(k) Cleared (K922901)
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Free shipping on orders over $99 · 30-day returns
Buckman Co., Inc.
Free shipping on orders over $99 · 30-day returns
INCISOR I PULSED ND:YAG LASER SYSTEM is an FDA 510(k)-cleared medical device (K922901) manufactured by Buckman Co., 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 19, 1992. Regulation: 8.
