Last synced on 14 November 2025 at 11:06 pm

PureLift

Page Type
Cleared 510(K)
510(k) Number
K190269
510(k) Type
Traditional
Applicant
Xtreem Pulse, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2019
Days to Decision
201 days
Submission Type
Summary

PureLift

Page Type
Cleared 510(K)
510(k) Number
K190269
510(k) Type
Traditional
Applicant
Xtreem Pulse, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2019
Days to Decision
201 days
Submission Type
Summary