Lca, Inc.
HYBRID SURGICAL DEVICE MODIFICATION
SKU K935258UPC GEX
In Stock
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IIFDA 510(k) Cleared (K935258)
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Free shipping on orders over $99 · 30-day returns
Lca, Inc.
Free shipping on orders over $99 · 30-day returns
HYBRID SURGICAL DEVICE MODIFICATION is an FDA 510(k)-cleared medical device (K935258) manufactured by Lca, 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 January 12, 1994. Regulation: 8.
