510(k) K823690

IVFLO-HP & IVFIL-HP by Tri-Med, Inc. — Product Code FPB

K823690 is an FDA 510(k) premarket notification submitted by Tri-Med, Inc. for the device "IVFLO-HP & IVFIL-HP". The FDA issued a decision of Substantially Equivalent on Dec 28, 1982. The device falls under product code FPB (Filter, Infusion Line), a Class II device regulated under 21 CFR 880.5440. Tri-Med, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Dec 28, 1982
Date Received
Dec 8, 1982
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