Last synced on 30 September 2022 at 11:05 pm

PureLift

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