Aesculap, Inc.
Caiman 5 Maryland
SKU K183180UPC GEI
In Stock
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IIFDA 510(k) Cleared (K183180)
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Free shipping on orders over $99 · 30-day returns
Aesculap, Inc.
Free shipping on orders over $99 · 30-day returns
Caiman 5 Maryland is an FDA 510(k)-cleared medical device (K183180) manufactured by Aesculap, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 11, 2019. Regulation: 8.
