510(k) K896203

SOLCOSEPT(TM) BLOOD TRANSFUSION FILTER by Solco Basle, Inc. — Product Code CAK

K896203 is an FDA 510(k) premarket notification submitted by Solco Basle, Inc. for the device "SOLCOSEPT(TM) BLOOD TRANSFUSION FILTER". The FDA issued a decision of Substantially Equivalent on February 1, 1990. The device falls under product code CAK (Microfilter, Blood Transfusion), a Class II device regulated under 21 CFR 880.5440. Solco Basle, Inc. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 1, 1990
Date Received
October 26, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Microfilter, Blood Transfusion
Device Class
Class II
Regulation Number
880.5440
Review Panel
HO
Submission Type