Aesculap, Inc.
AESCULAP PNEUMATIC KERRISON
SKU K062413UPC HAD
In Stock
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IIFDA 510(k) Cleared (K062413)
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Free shipping on orders over $99 · 30-day returns
Aesculap, Inc.
Free shipping on orders over $99 · 30-day returns
AESCULAP PNEUMATIC KERRISON is an FDA 510(k)-cleared medical device (K062413) manufactured by Aesculap, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 20, 2006. Regulation: 8.
