FDA 510(k) Applications Submitted by HEMOSPHERE INC

FDA 510(k) Number Submission Date Device Name Applicant
K120006 01/03/2012 HERO GRAFT HEMOSPHERE INC
K121532 05/24/2012 HERO GRAFT HEMOSPHERE INC
K091491 05/20/2009 HERO VASCULAR ACCESS DEVICE HEMOSPHERE INC


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