Device Classification Name |
System, Test, Immunological, Antigen, Tumor
More FDA Info for this Device |
510(K) Number |
K100344 |
Device Name |
System, Test, Immunological, Antigen, Tumor |
Applicant |
SIEMENS HEALTHCARE DIAGNOSTICS
MS 514, PO BOX 6101
NEWARK, DE 19714-6101 US
Other 510(k) Applications for this Company
|
Contact |
ROSE MARINELLI
Other 510(k) Applications for this Contact |
Regulation Number |
866.6010
More FDA Info for this Regulation Number |
Classification Product Code |
MOI
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
02/05/2010 |
Decision Date |
04/18/2011 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
IM - Immunology |
Review Advisory Committee |
IM - Immunology |
Statement / Summary / Purged Status |
Summary |
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|