Aesculap, Inc.
AESCULAP PRIMELINE CONTAINER LTD.
SKU K073168UPC KCT
In Stock
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IIFDA 510(k) Cleared (K073168)
1
Free shipping on orders over $99 · 30-day returns
Aesculap, Inc.
Free shipping on orders over $99 · 30-day returns
AESCULAP PRIMELINE CONTAINER LTD. is an FDA 510(k)-cleared medical device (K073168) manufactured by Aesculap, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 27, 2008. Regulation: 8.
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