| Device Type ID | 4113 |
| Device Name | Dilator, Cervical, Synthetic, Osmotic, Pregnancy Termination |
| Review Panel | Obstetrics/Gynecology |
| Premarket Review | Office Of Device Evaluation (ODE) Division Of Reproductive, Gastro-Renal, And Urological Devices (DRGUD) Obstetrics And Gynecology Devices Branch (OGDB) |
| Submission Type | PMA |
| FDA Device Classification | Class 3 Medical Device |
| Product Code | LOB |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 4113 |
| Device | Dilator, Cervical, Synthetic, Osmotic, Pregnancy Termination |
| Product Code | LOB |
| FDA Device Classification | Class 3 Medical Device |