510(k) K905794

PALL 3N1 FILTER by Pall Biomedical Products Co. — Product Code FPB

K905794 is an FDA 510(k) premarket notification submitted by Pall Biomedical Products Co. for the device "PALL 3N1 FILTER". The FDA issued a decision of Substantially Equivalent on June 13, 1991. The device falls under product code FPB (Filter, Infusion Line), 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
June 13, 1991
Date Received
December 27, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Filter, Infusion Line
Device Class
Class II
Regulation Number
880.5440
Review Panel
HO
Submission Type