Device Classification Name |
stent, ureteral
|
510(k) Number |
K180216 |
Device Name |
Seidmon Antegrade AQ Stent Set |
Applicant |
Cook Incorporated |
750 Daniels Way P.O. Box 489 |
Bloomington,
IN
47402
|
|
Applicant Contact |
Rebecca Odulio (Li-Chun-Liu) |
Correspondent |
Cook Incorporated |
750 Daniels Way P.O. Box 489 |
Bloomington,
IN
47402
|
|
Correspondent Contact |
Rebecca Odulio (Li-Chun-Liu) |
Regulation Number | 876.4620
|
Classification Product Code |
|
Date Received | 01/25/2018 |
Decision Date | 09/28/2018 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Gastroenterology/Urology
|
510k Review Panel |
Gastroenterology/Urology
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|