Device Classification Name |
catheter, angioplasty, peripheral, transluminal
|
510(k) Number |
K913391 |
Device Name |
TEGWIRE (TM) |
Applicant |
BOSTON SCIENTIFIC CORP. |
2710 ORCHARD PKWY. |
SAN JOSE,
CA
95134
|
|
Applicant Contact |
STEPHEN M PAGE |
Correspondent |
BOSTON SCIENTIFIC CORP. |
2710 ORCHARD PKWY. |
SAN JOSE,
CA
95134
|
|
Correspondent Contact |
STEPHEN M PAGE |
Regulation Number | 870.1250
|
Classification Product Code |
|
Date Received | 07/30/1991 |
Decision Date | 11/05/1991 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|