Device Classification Name |
catheter, angioplasty, peripheral, transluminal
|
510(k) Number |
K111899 |
Device Name |
ARMADA 35/35LL PTA CATHETER |
Applicant |
Abbott Vascular |
3200 Lakeside Drive |
Santa Clara,
CA
95054
|
|
Applicant Contact |
LAARNI RICAFORT |
Correspondent |
Abbott Vascular |
3200 Lakeside Drive |
Santa Clara,
CA
95054
|
|
Correspondent Contact |
LAARNI RICAFORT |
Regulation Number | 870.1250
|
Classification Product Code |
|
Subsequent Product Code |
|
Date Received | 07/05/2011 |
Decision Date | 10/03/2011 |
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
|
|
|