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LED Phototherapy Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162098
510(k) Type
Traditional
Applicant
Li-Tek Electronic Technology Corporation
Country
China
FDA Decision
Substantially Equivalent
Decision Date
1/30/2017
Days to Decision
185 days
Submission Type
Summary

LED Phototherapy Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162098
510(k) Type
Traditional
Applicant
Li-Tek Electronic Technology Corporation
Country
China
FDA Decision
Substantially Equivalent
Decision Date
1/30/2017
Days to Decision
185 days
Submission Type
Summary