Device Classification Name |
Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
More FDA Info for this Device |
510(K) Number |
K961181 |
Device Name |
Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass |
Applicant |
NALTIAC MEDICAL, INC.
17194 PRESTON RD.
SUITE 123-206
DALLAS, TX 75248 US
Other 510(k) Applications for this Company
|
Contact |
WENDEL LLOYD
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 |
03/26/1996 |
Decision Date |
06/21/1996 |
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 |
|