The following data is part of a premarket notification filed by Comeg Endoscopy with the FDA for Comeg Resectoscope And Laser-resectoscope Working Elements/urethrotomes/electrodes/albarrab Deflectors.
| Device ID | K971881 |
| 510k Number | K971881 |
| Device Name: | COMEG RESECTOSCOPE AND LASER-RESECTOSCOPE WORKING ELEMENTS/URETHROTOMES/ELECTRODES/ALBARRAB DEFLECTORS |
| Classification | Resectoscope |
| Applicant | COMEG ENDOSCOPY 13790 EAST RICE PLACE Aurora, CO 80015 |
| Contact | Kaelyn Hadley |
| Correspondent | Kaelyn Hadley COMEG ENDOSCOPY 13790 EAST RICE PLACE Aurora, CO 80015 |
| Product Code | FJL |
| Subsequent Product Code | EZO |
| Subsequent Product Code | FAS |
| Subsequent Product Code | FDC |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-05-20 |
| Decision Date | 1997-08-12 |
| Summary: | summary |