| K-number | K791977 |
| Device name | PSORALITE MARK I |
| Applicant | Paul B. Elder Co. |
| Product code | KGL |
| Device class | Class II |
| Decision date | Dec 28, 1979 |
| Decision | Substantially Equivalent |
| Regulation | 878.4630 |
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