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Laser treatment system , models Nyx plus, Grace plus, Nemesis, Ares

Page Type
Cleared 510(K)
510(k) Number
K211722
510(k) Type
Traditional
Applicant
Canadian Pioneer Medical Technology Corporation
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
2/25/2022
Days to Decision
266 days
Submission Type
Summary

Laser treatment system , models Nyx plus, Grace plus, Nemesis, Ares

Page Type
Cleared 510(K)
510(k) Number
K211722
510(k) Type
Traditional
Applicant
Canadian Pioneer Medical Technology Corporation
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
2/25/2022
Days to Decision
266 days
Submission Type
Summary