FDA 510(k) Applications Submitted by Selux Diagnostics, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K244044 | 12/30/2024 | PBC Separator with Selux AST System | Selux Diagnostics, Inc. |
| K211759 | 06/07/2021 | Selux AST System; Model AST Gen 1.0 | Selux Diagnostics, Inc. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact