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LED Spectrum therapy instrument

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231894
510(k) Type
Traditional
Applicant
Shenzhenshi Sincoheren S&T Development Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
9/20/2023
Days to Decision
84 days
Submission Type
Summary

LED Spectrum therapy instrument

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231894
510(k) Type
Traditional
Applicant
Shenzhenshi Sincoheren S&T Development Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
9/20/2023
Days to Decision
84 days
Submission Type
Summary