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CS1000 LIGHT THERAPY DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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