Device Classification Name |
Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
|
510(k) Number |
K981995 |
Device Name |
QUICKDRAW VENOUS CANNULA |
Applicant |
HEARTPORT, INC. |
700 BAY RD. |
REDWOOD CITY,
CA
94063
|
|
Applicant Contact |
MARIANNE C DRENNAN |
Correspondent |
HEARTPORT, INC. |
700 BAY RD. |
REDWOOD CITY,
CA
94063
|
|
Correspondent Contact |
MARIANNE C DRENNAN |
Regulation Number | 870.4210
|
Classification Product Code |
|
Date Received | 06/08/1998 |
Decision Date | 04/20/1999 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|