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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