Last synced on 14 November 2025 at 11:06 pm

PureLift Pro Edition

Page Type
Cleared 510(K)
510(k) Number
K230506
510(k) Type
Special
Applicant
Xtreem Pulse
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/2023
Days to Decision
117 days
Submission Type
Summary

PureLift Pro Edition

Page Type
Cleared 510(K)
510(k) Number
K230506
510(k) Type
Special
Applicant
Xtreem Pulse
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/2023
Days to Decision
117 days
Submission Type
Summary