The following data is part of a premarket notification filed by Vital Images, Inc. with the FDA for Vitreaview Software 6.1.
Device ID | K111892 |
510k Number | K111892 |
Device Name: | VITREAVIEW SOFTWARE 6.1 |
Classification | System, Image Processing, Radiological |
Applicant | VITAL IMAGES, INC. 5850 OPUS PARKWAY, SUITE 300 Minnetonka, MN 55343 -4414 |
Contact | Ian Nemerov |
Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2011-07-05 |
Decision Date | 2011-07-28 |
Summary: | summary |