Neothermia Corporation
NEOTHERMIA EN-BLOC BIOPSY SYSTEM
SKU K050737UPC GEI
In Stock
—
IIFDA 510(k) Cleared (K050737)
1
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Neothermia Corporation
Free shipping on orders over $99 · 30-day returns
NEOTHERMIA EN-BLOC BIOPSY SYSTEM is an FDA 510(k)-cleared medical device (K050737) manufactured by Neothermia Corporation. 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 30, 2005. Regulation: 8.
