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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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