Usa Laser Biotech, Inc. · Class II · Cleared Oct 28, 2009
| K-number | K091726 |
| Device name | NEXUS XPULSE 805 IR LAMP SYSTEM, NEXUS XPULSE 980 IR LAMP SYSTEM, MODEL 805, 980 |
| Applicant | Usa Laser Biotech, Inc. |
| Product code | ILY |
| Device class | Class II |
| Decision date | Oct 28, 2009 |
| Decision | Substantially Equivalent |
| Regulation | 890.5500 |
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