| Device Type ID | 5433 |
| Device Name | Applicator, Hyperthermia, Interstitial |
| Review Panel | Radiology |
| Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR) |
| Submission Type | PMA |
| FDA Device Classification | Class 3 Medical Device |
| Product Code | LMZ |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 5433 |
| Device | Applicator, Hyperthermia, Interstitial |
| Product Code | LMZ |
| FDA Device Classification | Class 3 Medical Device |