FDA 510(k) Applications Submitted by OMRIX BIOPHARMACEUTICALS LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K070575 02/28/2007 EVICEL APPLICATION DEVICE OMRIX BIOPHARMACEUTICALS LTD.
K090162 01/22/2009 EVICEL APPLICATION DEVICE OMRIX BIOPHARMACEUTICALS LTD.


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