FDA 510(k) Applications Submitted by Ralf de Andreis
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K191881 | 07/15/2019 | KBL 7000 alpha hybridSun, KBL 7900 alpha hybridSun, KBL 8000 alpha hybridSun | KBL GmbH |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact