Bard Peripheral Vascular
MODIFICATION TO G2 FILTER SYSTEM-FEMORAL DELIVERY KIT, MODEL RF-310F
SKU K062887UPC DTK
In Stock
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IIFDA 510(k) Cleared (K062887)
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Free shipping on orders over $99 · 30-day returns
Bard Peripheral Vascular
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO G2 FILTER SYSTEM-FEMORAL DELIVERY KIT, MODEL RF-310F is an FDA 510(k)-cleared medical device (K062887) manufactured by Bard Peripheral Vascular. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 25, 2006. Regulation: 8.
