American Laser Corp. · Class II · Cleared May 17, 1999
| K-number | K990665 |
| Device name | BQ/BM INTEGRATED LASER DELIVERY SYSTEM |
| Applicant | American Laser Corp. |
| Product code | HQF |
| Device class | Class II |
| Decision date | May 17, 1999 |
| Decision | Substantially Equivalent |
| Regulation | 886.4390 |
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