FDA 510(k) Applications Submitted by LIVETEC GMBH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K131797 | 06/18/2013 | 3B LASER NEEDLE | LIVETEC GMBH |
| K142215 | 08/12/2014 | Power Twin21-50/Power Twin21-100 | LIVETEC GMBH |
| K142722 | 09/23/2014 | 3B Laser 500, 3B Laser 200, LA-X P 500, LA-X P 200 | Livetec GMBH |
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