Last synced on 21 June 2024 at 11:04 pm

PureLift Pro Edition

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