510(k) K873667

PALL LEUKOCYTE REMOVAL FILTER, PLATELETS by Pall Biomedical Products Co. — Product Code CAK

K873667 is an FDA 510(k) premarket notification submitted by Pall Biomedical Products Co. for the device "PALL LEUKOCYTE REMOVAL FILTER, PLATELETS". The FDA issued a decision of Substantially Equivalent on January 6, 1988. The device falls under product code CAK (Microfilter, Blood Transfusion), a Class II device regulated under 21 CFR 880.5440. Pall Biomedical Products Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 6, 1988
Date Received
September 10, 1987
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