Last synced on 25 January 2026 at 3:41 am

Selux AST System; Model AST Gen 1.0

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211748
510(k) Type
Traditional
Applicant
Selux Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2023
Days to Decision
681 days
Submission Type
Summary

Selux AST System; Model AST Gen 1.0

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211748
510(k) Type
Traditional
Applicant
Selux Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2023
Days to Decision
681 days
Submission Type
Summary