Device Classification Name |
Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
More FDA Info for this Device |
510(K) Number |
K072556 |
Device Name |
Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass |
Applicant |
MERIT MEDICAL SYSTEMS, INC.
1600 WEST MERIT PKWY.
SOUTH JORDAN, UT 84095 US
Other 510(k) Applications for this Company
|
Contact |
SHIRLEY HYINK
Other 510(k) Applications for this Contact |
Regulation Number |
870.4290
More FDA Info for this Regulation Number |
Classification Product Code |
DTL
Other 510(k) Applications for this Device
More FDA Info for this Product Code |
Date Received |
09/10/2007 |
Decision Date |
11/20/2007 |
Decision |
SESE - SUBST EQUIV |
Classification Advisory Committee |
CV - Cardiovascular |
Review Advisory Committee |
CV - Cardiovascular |
Statement / Summary / Purged Status |
Summary |
Type |
Traditional |
Reviewed By Third Party |
N |
Expedited Review |
|