| Device |
device, fertility diagnostic, proceptive |
| Review Panel |
Obstetrics/Gynecology |
| Product Code | LHD |
|
Unclassified Reason
|
Pre-Amendment
|
| Submission Type |
510(k)
|
| Device Class |
Unclassified
|
| Total Product Life Cycle (TPLC) |
TPLC Product Code Report
|
| GMP Exempt? |
No
|
| Third Party Review |
Not Third Party Eligible |
|
|