| Device Type ID | 1933 |
| Device Name | Endoscope, Rigid |
| Regulation Description | Endoscope And Accessories. |
| 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) |
| CFR Regulation Number | 876.1500 [🔎] |
| FDA Device Classification | Class 2 Medical Device |
| Product Code | GCM |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Eligible For Accredited Persons Program |
| Device Type ID | 1933 |
| Device | Endoscope, Rigid |
| Product Code | GCM |
| FDA Device Classification | Class 2 Medical Device |
| Regulation Description | Endoscope And Accessories. |
| CFR Regulation Number | 876.1500 [🔎] |
| Device Problems | |
|---|---|
Poor Quality Image | 3 |
Material Fragmentation | 2 |
Break | 2 |
Microbial Contamination Of Device | 2 |
Adverse Event Without Identified Device Or Use Problem | 2 |
Endoscope | 2 |
Loss Of Or Failure To Bond | 1 |
Component Missing | 1 |
Tip | 1 |
Bent | 1 |
Insufficient Information | 1 |
Device Handling Problem | 1 |
Material Deformation | 1 |
| Total Device Problems | 20 |