510(k) K771826

INTRAVENOUS FILTER W/AUTO AIR VENT by Jelco Laboratories — Product Code FPB

K771826 is an FDA 510(k) premarket notification submitted by Jelco Laboratories for the device "INTRAVENOUS FILTER W/AUTO AIR VENT". The FDA issued a decision of Substantially Equivalent on October 13, 1977. The device falls under product code FPB (Filter, Infusion Line), a Class II device regulated under 21 CFR 880.5440. Jelco Laboratories has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 13, 1977
Date Received
September 19, 1977
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