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dermalux Flex MD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202028
510(k) Type
Traditional
Applicant
Aesthetic Technology Ltd
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
12/16/2020
Days to Decision
147 days
Submission Type
Summary

dermalux Flex MD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202028
510(k) Type
Traditional
Applicant
Aesthetic Technology Ltd
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
12/16/2020
Days to Decision
147 days
Submission Type
Summary