Sontek Corp.
PERIPHERAL TRANSLUMINAL ARGIOPLASTY
SKU K832279
In Stock
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FDA 510(k) Cleared (K832279)
1
Free shipping on orders over $99 · 30-day returns
Sontek Corp.
Free shipping on orders over $99 · 30-day returns
PERIPHERAL TRANSLUMINAL ARGIOPLASTY is an FDA 510(k)-cleared medical device (K832279) manufactured by Sontek Corp.. This device is classified under the Unknown specialty. FDA clearance granted on November 13, 1983.
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