Device Classification Name |
Method, Nephelometric, Immunoglobulins (G, A, M)
More FDA Info for this Device |
510(K) Number |
K061338 |
Device Name |
Method, Nephelometric, Immunoglobulins (G, A, M) |
Applicant |
DADE BEHRING, INC.
P.O. BOX 6101
NEWARK,, DE 19714 US
Other 510(k) Applications for this Company
|
Contact |
KATHLEEN DRAY-LYONS
Other 510(k) Applications for this Contact |
Regulation Number |
866.5510
More FDA Info for this Regulation Number |
Classification Product Code |
CFN
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
05/15/2006 |
Decision Date |
07/06/2006 |
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 |
|