Lightscalpel, Inc.
LIGHTSCALPEL LS-4020
SKU K213669UPC GEX
In Stock
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IIFDA 510(k) Cleared (K213669)
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Free shipping on orders over $99 · 30-day returns
Lightscalpel, Inc.
Free shipping on orders over $99 · 30-day returns
LIGHTSCALPEL LS-4020 is an FDA 510(k)-cleared medical device (K213669) manufactured by Lightscalpel, 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 14, 2023. Regulation: 8.
