FDA 510(k) Applications Submitted by LAURIE LYNCH
| 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 |
| K071778 | 07/02/2007 | HERO VASCULAR ACCESS DEVICE | GRAFTCATH INC. |
| K124039 | 12/28/2012 | HERO GRAFT | HEMOSHPERE, INC., A CRYOLIFE COMPANY |
| K131060 | 04/16/2013 | CLEARGUARD HD END CAP | PURSUIT VASCULAR, INC |
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