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FDA 510(k) Applications Submitted by MARIA PRANS 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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