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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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