Device Classification Name |
catheter, cannula and tubing, vascular, cardiopulmonary bypass
|
510(k) Number |
K171308 |
Device Name |
Tubing Pack |
Applicant |
Medtronic, Inc. |
8200 Coral Sea Street NE (MVS83) |
Mounds View,
MN
55112
|
|
Applicant Contact |
Renee Cveykus |
Correspondent |
Medtronic, Inc. |
8200 Coral Sea Street NE (MVS83) |
Mounds View,
MN
55112
|
|
Correspondent Contact |
Renee Cveykus |
Regulation Number | 870.4210
|
Classification Product Code |
|
Date Received | 05/03/2017 |
Decision Date | 06/02/2017 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Summary |
Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|