510(k) K904221

SEPACELL(R) PL-5A/10A LEUKOCYTE REMOVAL FILTERS by Baxter Healthcare Corp — Product Code CAK

K904221 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "SEPACELL(R) PL-5A/10A LEUKOCYTE REMOVAL FILTERS". The FDA issued a decision of Substantially Equivalent on October 26, 1990. The device falls under product code CAK (Microfilter, Blood Transfusion), a Class II device regulated under 21 CFR 880.5440. Baxter Healthcare Corp has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 26, 1990
Date Received
September 13, 1990
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