FDA 510(k) Applications Submitted by SLK Medical GmbH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K210913 | 03/29/2021 | V12 PRO | SLK Medical GmbH |
| K193476 | 12/16/2019 | VariLymph 12 pro | SLK Medical GmbH |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact