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Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240222
510(k) Type
Traditional
Applicant
Aesthetic Technology Ltd
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
6/4/2024
Days to Decision
130 days
Submission Type
Summary

Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240222
510(k) Type
Traditional
Applicant
Aesthetic Technology Ltd
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
6/4/2024
Days to Decision
130 days
Submission Type
Summary