Device Classification Name |
Filter, Intravascular, Cardiovascular
|
510(k) Number |
K760152 |
Device Name |
FILTER (7220&7221 MOBIN-UDDIN VENA CAVA) |
Applicant |
EDWARDS LABORATORIES |
4221 Richmond Rd., N.W. |
Walker,
MI
49534
|
|
Correspondent |
EDWARDS LABORATORIES |
4221 Richmond Rd., N.W. |
Walker,
MI
49534
|
|
Regulation Number | 870.3375
|
Classification Product Code |
|
Date Received | 07/01/1976 |
Decision Date | 07/19/1976 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|