Buckman Co., Inc. · Class II · Cleared Nov 20, 1992
| K-number | K922901 |
| Device name | INCISOR I PULSED ND:YAG LASER SYSTEM |
| Applicant | Buckman Co., Inc. |
| Product code | GEX |
| Device class | Class II |
| Decision date | Nov 20, 1992 |
| 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