The following data is part of a premarket notification filed by Prexion Corporation with the FDA for Prexion3d Excelsior.
Device ID | K173878 |
510k Number | K173878 |
Device Name: | PreXion3D Excelsior |
Classification | X-ray, Tomography, Computed, Dental |
Applicant | PreXion Corporation 1-14-1 Kandasuda-cho Chiyoda-ku, JP 101-0041 |
Contact | Katsumi Hayashi |
Correspondent | Katsumi Hayashi PreXion Corporation 1-14-1 Kandasuda-cho Chiyoda-ku, JP 101-0041 |
Product Code | OAS |
CFR Regulation Number | 892.1750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-12-21 |
Decision Date | 2018-01-19 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PREXION3D EXCELSIOR 87196223 5278056 Live/Registered |
PREXION CORPORATION 2016-10-07 |