# K060082: Tianjin Medis Disposable  Infusion Set

- Pathway: 510(k) (Abbreviated)
- Applicant: Tianjin Medis International Trade Co., Ltd.
- Decided: Mar 31, 2006 after 80 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
No predicates in its family tree.
4 later devices descend from it; 2 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K090012: Disposable Infusion Set (2009), 2 descendants of its own
- K234129: Ecomed Disposable Administration Sets (2024), 1 descendant of its own
- K254123: Ecomed Disposable Administration Sets (2026), 0 descendants of its own
- K090459: Disposable Tpe Infusion Set (2009), 0 descendants of its own

## Indications for use
Tianjin Medis Disposable Infusion set is a device intended to administer fluids from a container to a patient's vascular system through a catheter inserted into a vein.

Source page: https://510kreport.com/device/K060082
Methodology: https://510kreport.com/methodology