FDA 510(k) Applications Submitted by MARIA LILJEVRET
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K120884 | 03/23/2012 | PERICAM PSI | PERIMED AB |
| K131253 | 05/02/2013 | PERIFLUX 6000 | PERIMED AB |
| K152930 | 10/05/2015 | PeriFlux6000 | PERIMED AB |
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