FDA 510(k) Applications Submitted by MAICO DIAGNOSTICS GMBH

FDA 510(k) Number Submission Date Device Name Applicant
K171506 05/23/2017 Easyscreen Maico Diagnostics GmbH
K162210 08/05/2016 touchTymp MAICO DIAGNOSTICS GMBH


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact