FDA 510(k) Applications Submitted by VORTEX MEDICAL INC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K092486 | 08/13/2009 | VORTEX MEDICAL ANGIOVAC CARDIOPULMONARY BYPASS CIRCUIT | VORTEX MEDICAL INC |
| K091304 | 05/04/2009 | VORTEX CANNULA | VORTEX MEDICAL INC |
| K133445 | 11/12/2013 | ANGIOVAC CANNULA | VORTEX MEDICAL INC |
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