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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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