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GENTLEWAVES CONSUMER LED PHOTOMODULATION DEVICE

Page Type
Cleared 510(K)
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)
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