Device Classification Name |
set, administration, intravascular
|
510(k) Number |
K896161 |
Device Name |
AVI MODEL 2012, 1.2 MICRON FILTER IV ADMINISTRA. |
Applicant |
3M COMPANY |
1120 RED FOX RD. |
ST. PAUL,
MN
55112
|
|
Applicant Contact |
VON BUSCH |
Correspondent |
3M COMPANY |
1120 RED FOX RD. |
ST. PAUL,
MN
55112
|
|
Correspondent Contact |
VON BUSCH |
Regulation Number | 880.5440
|
Classification Product Code |
|
Date Received | 10/24/1989 |
Decision Date | 01/11/1990 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General Hospital
|
510k Review Panel |
General Hospital
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|