| Device Type ID | 3923 |
| Device Name | Forceps, Biopsy, Gynecological |
| Regulation Description | Obstetric-gynecologic Specialized Manual Instrument. |
| 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 | 510(K) Exempt |
| CFR Regulation Number | 884.4530 [🔎] |
| FDA Device Classification | Class 1 Medical Device |
| Product Code | HFB |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 3923 |
| Device | Forceps, Biopsy, Gynecological |
| Product Code | HFB |
| FDA Device Classification | Class 1 Medical Device |
| Regulation Description | Obstetric-gynecologic Specialized Manual Instrument. |
| CFR Regulation Number | 884.4530 [🔎] |
| Device Problems | |
|---|---|
Difficult To Open Or Close | 6 |
Failure To Deliver Energy | 4 |
Activation, Positioning Or Separation Problem | 2 |
Failure To Fire | 2 |
Retraction Problem | 1 |
Sticking | 1 |
Failure To Conduct | 1 |
Flaked | 1 |
Insufficient Information | 1 |
| Total Device Problems | 19 |