510(k) K771536

AIR VENT FILTER NEEDLE, 0.45 by Jelco Laboratories — Product Code FPB

K771536 is an FDA 510(k) premarket notification submitted by Jelco Laboratories for the device "AIR VENT FILTER NEEDLE, 0.45". The FDA issued a decision of Substantially Equivalent on October 25, 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 25, 1977
Date Received
August 10, 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