Device Classification Name |
Microscope,Automated,Image Analysis,Immunohistochemistry,Operator Intervention,Nuclear Intensity & Percent Positivity
More FDA Info for this Device |
510(K) Number |
K050012 |
Device Name |
Microscope,Automated,Image Analysis,Immunohistochemistry,Operator Intervention,Nuclear Intensity & Percent Positivity |
Applicant |
TRIPATH IMAGING, INC.
780 PLANTATION DR.
BURLINGTON, NC 27215 US
Other 510(k) Applications for this Company
|
Contact |
BRYAN TUCKER
Other 510(k) Applications for this Contact |
Regulation Number |
864.1860
More FDA Info for this Regulation Number |
Classification Product Code |
NQN
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
01/03/2005 |
Decision Date |
05/06/2005 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
HE - Hematology |
Review Advisory Committee |
PA - Pathology |
Statement / Summary / Purged Status |
Statement |
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|