The following data is part of a premarket notification filed by Fujifilm Corporation with the FDA for Fujifilm Ultrasonic Endoscope.
| Device ID | K183433 |
| 510k Number | K183433 |
| Device Name: | FUJIFILM Ultrasonic Endoscope |
| Classification | Endoscopic Ultrasound System, Gastroenterology-urology |
| Applicant | Fujifilm Corporation 798 Miyanodai Kaisei-Machi Ashigarakami-gun, JP 258-8538 |
| Contact | Randy Vader |
| Correspondent | Jeffrey Wan Fujifilm Medical Systems U.S.A., Inc. 81 Hartwell Avenue, Suite 300 Lexington, MA 02421 |
| Product Code | ODG |
| Subsequent Product Code | FDS |
| Subsequent Product Code | ITX |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-12-11 |
| Decision Date | 2019-09-05 |
| Summary: | summary |