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CS1000 LIGHT THERAPY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K110558
510(k) Type
Traditional
Applicant
GENESIS HEALTH LIGHT CORPORATION
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
7/12/2012
Days to Decision
500 days
Submission Type
Summary

CS1000 LIGHT THERAPY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K110558
510(k) Type
Traditional
Applicant
GENESIS HEALTH LIGHT CORPORATION
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
7/12/2012
Days to Decision
500 days
Submission Type
Summary