| Device Type ID | 1710 |
| Device Name | Urethrotome |
| Regulation Description | Urethrotome. |
| Regulation Medical Specialty | Gastroenterology/Urology |
| Review Panel | Gastroenterology/Urology |
| Premarket Review | Office Of Device Evaluation (ODE) Division Of Reproductive, Gastro-Renal, And Urological Devices (DRGUD) Urology And Lithotripsy Devices Branch (ULDB) |
| Submission Type | 510(K) Exempt |
| CFR Regulation Number | 876.4770 [🔎] |
| FDA Device Classification | Class 2 Medical Device |
| Product Code | EZO |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Eligible For Accredited Persons Expansion Pilot Program |
| Device Type ID | 1710 |
| Device | Urethrotome |
| Product Code | EZO |
| FDA Device Classification | Class 2 Medical Device |
| Regulation Description | Urethrotome. |
| CFR Regulation Number | 876.4770 [🔎] |
| Device Problems | |
|---|---|
Material Separation | 1 |
Break | 1 |
Adverse Event Without Identified Device Or Use Problem | 1 |
| Total Device Problems | 3 |