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Diode laser therapy device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212734
510(k) Type
Traditional
Applicant
TRIANGEL RSD LIMITED
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/6/2023
Days to Decision
645 days
Submission Type
Summary

Diode laser therapy device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212734
510(k) Type
Traditional
Applicant
TRIANGEL RSD LIMITED
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/6/2023
Days to Decision
645 days
Submission Type
Summary