Sorenson Laboratories, Inc. · Class II · Cleared Jun 4, 1992
| K-number | K920597 |
| Device name | HANDI-LASE CO2 SURGICAL LASER INSTRUMENT |
| Applicant | Sorenson Laboratories, Inc. |
| Product code | GEX |
| Device class | Class II |
| Decision date | Jun 4, 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