Oberon GmbH Fiber Technologies · Class II · Cleared Oct 15, 2014
| K-number | K140470 |
| Device name | OBERON: LASER SURGERY FIBER, ATRAUMATIC SURGERY FIBER, SIDE FIRE FIBER, RADIAL EMISSION FIBER, DENTAL SURGERY FIBER |
| Applicant | Oberon GmbH Fiber Technologies |
| Product code | GEX |
| Device class | Class II |
| Decision date | Oct 15, 2014 |
| 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