Device |
rf/microwave hyperthermia system, cancer treatment |
Definition |
Used in conjunction with radiation therapy for the treatment of cervical carcinoma patients who normally would be treated with combined chemotherapy and radiation but are ineligible for chemotherapy due to patient related factors. |
Physical State |
Hyperthermia System |
Technical Method |
Hyperthermia |
Target Area |
Cervical carcinoma |
Review Panel |
Obstetrics/Gynecology |
Product Code | PAS |
Premarket Review |
Reproductive, Gynecology and Urology Devices
(DHT3B)
Reproductive, Gynecology and Urology Devices
(DHT3B)
|
Submission Type |
HDE - Humanitarian Device Exemption
|
Device Class |
HDE
|
Total Product Life Cycle (TPLC) |
TPLC Product Code Report
|
GMP Exempt? |
No
|
Summary Malfunction Reporting |
Ineligible |
Implanted Device? |
No
|
Life-Sustain/Support Device? |
No
|
Third Party Review |
Not Third Party Eligible |
|
|