Device Classification Name |
system, balloon, intra-aortic and control
|
510(k) Number |
K993966 |
Device Name |
8FR. NARROWFLEX UNIVERSAL INTRA-AORTIC BALLOON CATHETER |
Applicant |
ARROW INTL., INC. |
9 PLYMOUTH ST. |
EVERETT,
MA
02149
|
|
Applicant Contact |
WILLIAM PAQUIN |
Correspondent |
ARROW INTL., INC. |
9 PLYMOUTH ST. |
EVERETT,
MA
02149
|
|
Correspondent Contact |
WILLIAM PAQUIN |
Regulation Number | 870.3535
|
Classification Product Code |
|
Date Received | 11/23/1999 |
Decision Date | 02/18/2000 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Summary |
Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|