| Device Type ID | 4112 |
| Device Name | Catheter, Sampling, Chorionic Villus |
| 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 | LLX |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 4112 |
| Device | Catheter, Sampling, Chorionic Villus |
| Product Code | LLX |
| FDA Device Classification | Class 3 Medical Device |
| Device Problems | |
|---|---|
Burst Container Or Vessel | 1 |
Programming Issue | 1 |
| Total Device Problems | 2 |