Sandstone Medical Technologies, LLC · Class II · Cleared Feb 3, 2009
| K-number | K082407 |
| Device name | MODIFICATION TO ULTRALIGHT II ND: YAG LASER SYSTEM |
| Applicant | Sandstone Medical Technologies, LLC |
| Product code | GEX |
| Device class | Class II |
| Decision date | Feb 3, 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