ETHICON, Inc.
MODIFIED E-PACK PROCEDURE KIT
SKU K970317UPC GAM
In Stock
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IIFDA 510(k) Cleared (K970317)
1
Free shipping on orders over $99 · 30-day returns
ETHICON, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFIED E-PACK PROCEDURE KIT is an FDA 510(k)-cleared medical device (K970317) manufactured by ETHICON, 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 April 24, 1997. Regulation: 8.
