| Device Type ID | 3922 |
| Device Name | Amnioscope, Transabdominal (fetoscope) (and Accessories) |
| Regulation Description | Transabdominal Amnioscope (fetoscope) And Accessories. |
| Regulation Medical Specialty | Obstetrics/Gynecology |
| 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 | HDE - Humanitarian Device Exem |
| CFR Regulation Number | 884.1600 [🔎] |
| FDA Device Classification | Class HDE Medical Device |
| Product Code | HFA |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 3922 |
| Device | Amnioscope, Transabdominal (fetoscope) (and Accessories) |
| Product Code | HFA |
| Regulation Description | Transabdominal Amnioscope (fetoscope) And Accessories. |
| CFR Regulation Number | 884.1600 [🔎] |