510(k) K896664

MODIFIED SEPACELL PL-SERIES LEUKOCYTE REMOVAL FILT by Asahi Medical Co., Ltd. — Product Code CAK

K896664 is an FDA 510(k) premarket notification submitted by Asahi Medical Co., Ltd. for the device "MODIFIED SEPACELL PL-SERIES LEUKOCYTE REMOVAL FILT". The FDA issued a decision of Substantially Equivalent on January 24, 1990. The device falls under product code CAK (Microfilter, Blood Transfusion), a Class II device regulated under 21 CFR 880.5440. Asahi Medical Co., Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 24, 1990
Date Received
November 24, 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