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FDA 510(k) Applications Submitted by TOUL MEDITECH AB
FDA 510(k) Number
Submission Date
Device Name
Applicant
K190027
01/07/2019
SteriStay
Toul Meditech AB
K173349
10/25/2017
Operio
Toul Meditech AB
K153498
12/07/2015
Operio
TOUL MEDITECH AB
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