Pacesetter Systems
DIRECTIONAL BOOT
SKU K813150UPC DXY
In Stock
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IIIFDA 510(k) Cleared (K813150)
1
Free shipping on orders over $99 · 30-day returns
Pacesetter Systems
Free shipping on orders over $99 · 30-day returns
DIRECTIONAL BOOT is an FDA 510(k)-cleared medical device (K813150) manufactured by Pacesetter Systems. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on December 1, 1981. Regulation: 8.
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