The following data is part of a premarket notification filed by Barco Nv with the FDA for Barco Mwd 321 Plus Medical Workstation Display.
Device ID | K000292 |
510k Number | K000292 |
Device Name: | BARCO MWD 321 PLUS MEDICAL WORKSTATION DISPLAY |
Classification | System, Image Processing, Radiological |
Applicant | BARCO NV P.O. BOX 12038 La Jolla, CA 92039 -2038 |
Contact | Frank Ferguson |
Correspondent | Frank Ferguson BARCO NV P.O. BOX 12038 La Jolla, CA 92039 -2038 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-01-31 |
Decision Date | 2000-03-29 |