FDA 510(k) Applications Submitted by Storz Medical AG
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K202112 | 07/30/2020 | Storz Medical Duolith SD1 T-Top & Tower System with C-Actor Sepia Handpiece | Storz Medical AG |
| K173692 | 12/01/2017 | D-Actor 200 Vibration Massage System | Storz Medical AG |
| K203710 | 12/21/2020 | Storz Medical MAGNETOLITH Muscle Stimulator | Storz Medical AG |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact