FDA 510(k) Applications Submitted by VITROLIFE AB
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K032154 | 07/14/2003 | G-FREEZEKIT BLAST | VITROLIFE AB |
| K032155 | 07/14/2003 | G-THAWKIT BLAST | VITROLIFE AB |
| K022730 | 08/16/2002 | PERFADEX SOLUTION FOR LUNG PRESERVATION | VITROLIFE AB |
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