Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by NORDICNEUROLAB
FDA 510(k) Number
Submission Date
Device Name
Applicant
K092253
07/28/2009
MODIFICATION TO FMRI HARDWARE SYSTEM
NORDICNEUROLAB
K140956
04/14/2014
LCD MONITOR
NORDICNEUROLAB
K123306
10/24/2012
NORDIC TUMOREX
NORDICNEUROLAB
K133910
12/23/2013
NORDICBRAINEX
NORDICNEUROLAB
K073099
11/02/2007
FMRI HARDWARE SYSTEM
NORDICNEUROLAB
K080515
02/25/2008
FMRI HARDWARE SYSTEM
NORDICNEUROLAB
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact