FDA 510(k) Applications Submitted by WILLIAM PAQUIN
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K010330 |
02/02/2001 |
ARROW REDIGUARD, 9FR. 50CC, INTRA-AORTIC BALLOON VATHETER, IAB-R950-U |
ARROW INTL., INC. |
K000729 |
03/06/2000 |
ARROW ULTRA 8 INTRA-AORTIC BALLOON CATHETERS (IABS) 8FR 30CC AND 40CC UNIVERSAL |
ARROW INTL., INC. |
K040801 |
03/29/2004 |
INTRA-AORTIC BALLOON (IAB) |
ARROW INTL., INC. |
K021462 |
05/07/2002 |
ARROW INTRA-AORTIC BALLOON (IAB) CATHETER WITH A FIBER OPTIC SENSOR AND A MEASUREMENT SYSTEM, MODELS IAB-05830-F,IAB5840 |
ARROW INTL., INC. |
K002256 |
07/25/2000 |
ARROW ACAT 2 INTRA-AORTIC BALLOON PUMP |
ARROW INTL., INC. |
K993966 |
11/23/1999 |
8FR. NARROWFLEX UNIVERSAL INTRA-AORTIC BALLOON CATHETER |
ARROW INTL., INC. |
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