Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K141865
Device Classification Name
Recorder, Attention Task Performance
More FDA Info for this Device
510(K) Number
K141865
Device Name
Recorder, Attention Task Performance
Applicant
ANTHROTRONIX, INC
8737 COLESVILLE ROAD
SUITE L-203
SILVER SPRING, MD 20910 US
Other 510(k) Applications for this Company
Contact
CORINA E LATHAN, PHD, PE
Other 510(k) Applications for this Contact
Regulation Number
000.0000
More FDA Info for this Regulation Number
Classification Product Code
LQD
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
07/10/2014
Decision Date
10/15/2014
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
-
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact