Last synced on 20 December 2024 at 11:05 pm

PureLift Pro Plus

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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