# K121269: TBA

- Pathway: 510(k) (Traditional)
- Applicant: Migada Plant
- Decided: Jan 22, 2013 after 271 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.
2 later devices descend from it; 2 cite 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)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K201142: TEVADAPTOR Bag Adaptor LL, TEVADAPTOR Bag Adaptor LL with ULTRASITE, TEVADAPTOR Bag Adaptor SP with ULTRASITE, TEVADAPTOR IV Secondary Safety Set with ULTRASITE, TEVADAPTOR IV Secondary Safety set (2021), 0 descendants of its own
- K141306: Tevadaptor; Connecting Set W/ Ultrasite Injection Site, Spike Port Adaptor Set W/ Ultrasite Injection Site (2014), 0 descendants of its own

## Indications for use
The LV. Administration Set is a single use, sterile L-V. set for administration of drugs and/ or fluids from a container to a patient vascular system.

Source page: https://510kreport.com/device/K121269
Methodology: https://510kreport.com/methodology