FDA 510(k) Applications Submitted by Dietmar Fischer
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K090762 | 03/23/2009 | LEDA | QUANTEL DERMA GMBH |
| K221623 | 06/06/2022 | FlexSys, FlexSys UVB EPL 308 nm, FlexSys UVB EPL lite 308 nm, FlexSys IR 1550 nm | GME German Medical Engineering GmbH |
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