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GENTLEWAVES CONSUMER LED PHOTOMODULATION DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062991
510(k) Type
Traditional
Applicant
Light Bioscience, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2008
Days to Decision
504 days
Submission Type
Summary

GENTLEWAVES CONSUMER LED PHOTOMODULATION DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062991
510(k) Type
Traditional
Applicant
Light Bioscience, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/15/2008
Days to Decision
504 days
Submission Type
Summary