Aesculap, Inc.
AESCULAP NEEDLESCOPIC INSTRUMENT SYSTEM
SKU K982623UPC GCJ
In Stock
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IIFDA 510(k) Cleared (K982623)
1
Free shipping on orders over $99 · 30-day returns
Aesculap, Inc.
Free shipping on orders over $99 · 30-day returns
AESCULAP NEEDLESCOPIC INSTRUMENT SYSTEM is an FDA 510(k)-cleared medical device (K982623) manufactured by Aesculap, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 29, 1998. Regulation: 8.
