Device Classification Name |
ligator, hemorrhoidal
|
510(k) Number |
K963166 |
Device Name |
O'REGAN LIGATOR |
Applicant |
PATRICK J. O'REGAN |
912 - 750 WEST BROADWAY |
VANCOUVER,
CA
V5Z 1H8
|
|
Applicant Contact |
PATRICK J O'REGAN |
Correspondent |
PATRICK J. O'REGAN |
912 - 750 WEST BROADWAY |
VANCOUVER,
CA
V5Z 1H8
|
|
Correspondent Contact |
PATRICK J O'REGAN |
Regulation Number | 876.4400
|
Classification Product Code |
|
Date Received | 08/14/1996 |
Decision Date | 05/05/1997 |
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
|
|
|