Last synced on 14 November 2025 at 11:06 pm

PureLift GLOW

Page Type
Cleared 510(K)
510(k) Number
K243587
510(k) Type
Traditional
Applicant
Xtreem Pulse LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2025
Days to Decision
106 days
Submission Type
Summary

PureLift GLOW

Page Type
Cleared 510(K)
510(k) Number
K243587
510(k) Type
Traditional
Applicant
Xtreem Pulse LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2025
Days to Decision
106 days
Submission Type
Summary