# K955821: I.V. Administration Sets

- Pathway: 510(k) (Traditional)
- Applicant: Medical Associates Network, Inc.
- Decided: Jul 10, 1996 after 197 days
- Product code: FPA (Set, Administration, Intravascular)
- Device class: 2
- Regulation: 21 CFR 880.5440
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K860605 (1986). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K944320: Vented/Non-Vented Gemini Administration Set, Imed Corp. (1995) Summary page 1.
- K860605: Filter Set 1) 1.2 Mic Filter 2) 3.0 Mic Filter, Migada, Ltd. (1986) Summary page 1.

## Most influential descendants
- K962801: Safe Mate I.V. Extension Sets (1996), 0 descendants of its own

## Indications for use
The I.V. Administration Sets of this Notification provide a means for administering Parenteral solutions from a standard solution container intravenously to a patient.

Source page: https://510kreport.com/device/K955821
Methodology: https://510kreport.com/methodology
