Last synced on 17 May 2024 at 11:06 pm

Xtrallux Alpha (XA136R-USA), Xtrallux Super Plus (XS276R-USA/XS276L-USA), Xtrallux Turbo Pro (XP316R-USA), Xtrallux Extreme RX (XR352R-USA)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222364
510(k) Type
Traditional
Applicant
Xtrallux, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2022
Days to Decision
104 days
Submission Type
Summary

Xtrallux Alpha (XA136R-USA), Xtrallux Super Plus (XS276R-USA/XS276L-USA), Xtrallux Turbo Pro (XP316R-USA), Xtrallux Extreme RX (XR352R-USA)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222364
510(k) Type
Traditional
Applicant
Xtrallux, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2022
Days to Decision
104 days
Submission Type
Summary