Device Classification Name |
Tubes, Vials, Systems, Serum Separators, Blood Collection
More FDA Info for this Device |
510(K) Number |
K971239 |
Device Name |
Tubes, Vials, Systems, Serum Separators, Blood Collection |
Applicant |
GREINER AMERICA, INC.
P.O. BOX 953279
LAKE MARY, FL 32795-3279 US
Other 510(k) Applications for this Company
|
Contact |
ED MAIER
Other 510(k) Applications for this Contact |
Regulation Number |
862.1675
More FDA Info for this Regulation Number |
Classification Product Code |
JKA
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
04/02/1997 |
Decision Date |
05/12/1997 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
CH - Clinical Chemistry |
Review Advisory Committee |
CH - Clinical Chemistry |
Statement / Summary / Purged Status |
Summary |
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|