| K-number | K912249 |
| Device name | PATIENT DOSE MONITOR |
| Applicant | Theta Systems, Inc. |
| Product code | KPZ |
| Device class | Class II |
| Decision date | Aug 30, 1991 |
| Decision | Substantially Equivalent |
| Regulation | 892.5900 |
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