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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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