Device Classification Name |
microfilter, blood transfusion
|
510(k) Number |
BK000045 |
Tradename |
Imugard III-PL
|
Device Name |
Microfilter, Blood Transfusion |
Original Applicant |
Terumo Medical Corporation |
125 blue ball road |
elkton,
MD
21921
|
|
Regulation Number | 880.5440
|
Classification Product Code |
|
Date Received | 11/20/2000 |
Decision Date | 09/28/2001 |
Decision |
substantially equivalent (SE) |
Classification Advisory Committee |
General Hospital
|
Review Advisory Committee |
General Hospital
|
Type |
510(k) Traditional
|
Total Product Life Cycle (TPLC) |
TPLC Device Report
|
Reviewed by Third Party |
No
|
Expedited Review |
No
|
Combination Product |
No
|
In Vitro Product |
No
|
|
|