Biolitec Medical Devices, Inc. · Class II · Cleared Sep 6, 2011
| K-number | K112324 |
| Device name | CERALAS 980NM DIODE LASER FAMILY |
| Applicant | Biolitec Medical Devices, Inc. |
| Product code | GEX |
| Device class | Class II |
| Decision date | Sep 6, 2011 |
| 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