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OMNILUX REVIVE AND OMNILUX PLUS

Page Type
Cleared 510(K)
510(k) Number
K050216
510(k) Type
Traditional
Applicant
PHOTO THERAPEUTICS LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/9/2005
Days to Decision
190 days
Submission Type
Summary

OMNILUX REVIVE AND OMNILUX PLUS

Page Type
Cleared 510(K)
510(k) Number
K050216
510(k) Type
Traditional
Applicant
PHOTO THERAPEUTICS LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/9/2005
Days to Decision
190 days
Submission Type
Summary