The following data is part of a premarket notification filed by American Optical Corp. with the FDA for Ao Flexible Fiber Optic S/colonoscope.
| Device ID | K792179 |
| 510k Number | K792179 |
| Device Name: | AO FLEXIBLE FIBER OPTIC S/COLONOSCOPE |
| Classification | Colonoscope And Accessories, Flexible/rigid |
| Applicant | AMERICAN OPTICAL CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FDF |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-10-29 |
| Decision Date | 1979-12-06 |