Last synced on 14 November 2025 at 11:06 pm

PureLift Pro Plus

Page Type
Cleared 510(K)
510(k) Number
K221443
510(k) Type
Special
Applicant
Xtreem Pulse LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2022
Days to Decision
156 days
Submission Type
Summary

PureLift Pro Plus

Page Type
Cleared 510(K)
510(k) Number
K221443
510(k) Type
Special
Applicant
Xtreem Pulse LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2022
Days to Decision
156 days
Submission Type
Summary