Laser Centers of America, Inc.
HYBRID SURGICAL DEVICES, MODIFICIATION
SKU K951353UPC GEI
In Stock
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IIFDA 510(k) Cleared (K951353)
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Free shipping on orders over $99 · 30-day returns
Laser Centers of America, Inc.
Free shipping on orders over $99 · 30-day returns
HYBRID SURGICAL DEVICES, MODIFICIATION is an FDA 510(k)-cleared medical device (K951353) manufactured by Laser Centers of America, 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 April 5, 1995. Regulation: 8.
