Device Classification Name |
stent, ureteral
|
510(k) Number |
K864225 |
Device Name |
ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT |
Applicant |
ANGIOMED U.S., INC. |
4081 EAST LA PALMA AVE., |
SUITE E |
ANAHEIM,
CA
92807
|
|
Applicant Contact |
RICHARD P MOHR |
Correspondent |
ANGIOMED U.S., INC. |
4081 EAST LA PALMA AVE., |
SUITE E |
ANAHEIM,
CA
92807
|
|
Correspondent Contact |
RICHARD P MOHR |
Regulation Number | 876.4620
|
Classification Product Code |
|
Date Received | 10/28/1986 |
Decision Date | 01/30/1987 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Gastroenterology/Urology
|
510k Review Panel |
Gastroenterology/Urology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|