Dornier Medtech America, Inc. · Class II · Cleared Aug 19, 2002
| K-number | K021724 |
| Device name | DORNIER DIODE LASER FAMILY, INCLUDING MEDILAS D FIBERTOM, MEDILAS D SKINPULSE & MEDILAS D SKINPULSE S LASER SYSTEMS |
| Applicant | Dornier Medtech America, Inc. |
| Product code | GEX |
| Device class | Class II |
| Decision date | Aug 19, 2002 |
| Decision | Substantially Equivalent |
| Regulation | 878.4810 |
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