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 |