Wm.I.Kern & Co., Inc. · Class II · Cleared May 14, 1992
| K-number | K920004 |
| Device name | PBI MULTILASE D COPPER VAPOR LASER |
| Applicant | Wm.I.Kern & Co., Inc. |
| Product code | GEX |
| Device class | Class II |
| Decision date | May 14, 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