| Device |
device, occlusion, tubal, contraceptive |
| Regulation Description |
Contraceptive tubal occlusion device (TOD) and introducer. |
| Definition |
Call for pmas to be filed by 12/30/87 (52 fr 36883 (10/1/87)). |
| Regulation Medical Specialty |
Obstetrics/Gynecology |
| Review Panel |
Obstetrics/Gynecology |
| Product Code | KNH |
| Submission Type |
PMA
|
| Regulation Number |
884.5380
|
| Device Class |
3
|
| Total Product Life Cycle (TPLC) |
TPLC Product Code Report
|
| GMP Exempt? |
No
|
| Third Party Review |
Not Third Party Eligible |
|
|