Plasiatek, LLC
PLASIATEK ACTUATOR
SKU K041917UPC BTR
In Stock
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IIFDA 510(k) Cleared (K041917)
1
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Plasiatek, LLC
Free shipping on orders over $99 · 30-day returns
PLASIATEK ACTUATOR is an FDA 510(k)-cleared medical device (K041917) manufactured by Plasiatek, LLC. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 6, 2005. Regulation: 8.
