Dornier Medtech America, Inc. · Class II · Cleared Jan 30, 2009
| K-number | K083258 |
| Device name | MEDILAS D FAMILY LASERS, INCLUDING MEDILAS D LITEBEAM, LITEBEAM +, UROBEAM, MULTIBEAM, FLEXIPULSE AND MAGNAPULSE |
| Applicant | Dornier Medtech America, Inc. |
| Product code | GEX |
| Device class | Class II |
| Decision date | Jan 30, 2009 |
| Decision | Substantially Equivalent |
| Regulation | 878.4810 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov