Device Classification Name |
Antigens, Febrile, Slide And Tube, All Groups, Salmonella Spp.
More FDA Info for this Device |
510(K) Number |
K955209 |
Device Name |
Antigens, Febrile, Slide And Tube, All Groups, Salmonella Spp. |
Applicant |
SA SCIENTIFIC, INC.
4919 GOLDEN QUAIL
SAN ANTONIO, TX 78240 US
Other 510(k) Applications for this Company
|
Contact |
HARBI SHADFAN
Other 510(k) Applications for this Contact |
Regulation Number |
866.3550
More FDA Info for this Regulation Number |
Classification Product Code |
GNC
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
11/14/1995 |
Decision Date |
02/02/1996 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
MI - Microbiology |
Review Advisory Committee |
MI - Microbiology |
Statement / Summary / Purged Status |
Statement |
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|