FDA 510(k) Applications Submitted by QUANTEL DERMA GMBH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K090762 | 03/23/2009 | LEDA | QUANTEL DERMA GMBH |
| K090639 | 03/10/2009 | EXELO2, MODEL 4010 | QUANTEL DERMA GMBH |
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