FDA 510(k) Applications Submitted by Canadian Pioneer Medical Technology Corporation

FDA 510(k) Number Submission Date Device Name Applicant
K212793 09/01/2021 Laser Treatment System, Model: Hera, Armo Canadian Pioneer Medical Technology Corporation
K211722 06/04/2021 Laser treatment system , models Nyx plus, Grace plus, Nemesis, Ares Canadian Pioneer Medical Technology Corporation
K210033 01/05/2021 Laser Treatment System, Model: NYX and Grace Canadian Pioneer Medical Technology Corporation


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