Padpro, LLC
PADPRO MODEL #2516
SKU K020203UPC MKJ
In Stock
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IIIFDA 510(k) Cleared (K020203)
1
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Padpro, LLC
Free shipping on orders over $99 · 30-day returns
PADPRO MODEL #2516 is an FDA 510(k)-cleared medical device (K020203) manufactured by Padpro, LLC. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on May 7, 2002. Regulation: 8.
