# K970255: Kipp Med I.V. Manifold

- Pathway: 510(k) (Traditional)
- Applicant: The Kipp Group
- Decided: Apr 14, 1997 after 82 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 K942391 (1995). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K942391: Braun Manifold, B.Braun Medical, Inc. (1995) Summary page 1.

## Most influential descendants
- K071421: Promepla Intravascular Administration Set and Extension Set (2007), 0 descendants of its own

## Indications for use
This device is intended to be used as a conduit for the delivery of I.V. fluids from a container to a patient's vascular system through a needle or catheter inserted into a vein. Additionally, this device is intended to serve as an injection site for other infusion fluids. This device is intended to be used only by trained professionals in a clinical or hospital environment.

Source page: https://510kreport.com/device/K970255
Methodology: https://510kreport.com/methodology