Name: CROSSEAL APPLICATION DEVICE
Brand: Omrix Biopharmaceuticals, Inc.
SKU: K030032

CROSSEAL APPLICATION DEVICE is an FDA 510(k)-cleared medical device (K030032) manufactured by Omrix Biopharmaceuticals, 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 March 20, 2003. Regulation: 8.

CROSSEAL APPLICATION DEVICE

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