Device Classification Name |
System, Test, Automated, Antimicrobial Susceptibility, Short Incubation
More FDA Info for this Device |
510(K) Number |
K032399 |
Device Name |
System, Test, Automated, Antimicrobial Susceptibility, Short Incubation |
Applicant |
BIOMERIEUX, INC.
595 ANGLUM DR.
HAZELWOOD, MO 63042-2320 US
Other 510(k) Applications for this Company
|
Contact |
Nancy Weaver
Other 510(k) Applications for this Contact |
Regulation Number |
866.1645
More FDA Info for this Regulation Number |
Classification Product Code |
LON
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
08/04/2003 |
Decision Date |
09/10/2003 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
MI - Microbiology |
Review Advisory Committee |
MI - Microbiology |
Statement / Summary / Purged Status |
Summary |
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|