Device Classification Name |
clamp, surgical, general & plastic surgery
|
510(k) Number |
K800074 |
Device Name |
VESSEL OCCLUDER |
Applicant |
CORDIS CORP. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
CORDIS CORP. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 878.4800
|
Classification Product Code |
|
Date Received | 01/14/1980 |
Decision Date | 01/28/1980 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General & Plastic Surgery
|
510k Review Panel |
General & Plastic Surgery
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|