# K092984: Panpac Uterine Inector, Model UI-4.0, UI-2.0

- Pathway: 510(k) (Traditional)
- Applicant: Panpac Medical Corporation
- Decided: Apr 7, 2010 after 191 days
- Product code: LKF (Cannula, Manipulator/Injector, Uterine)
- Device class: 2
- Regulation: 21 CFR 884.4530
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Indications for use
To be used during hysterosonography, hysterosalpingogram, salpingoplasties, and hydrotubation.

Source page: https://510kreport.com/device/K092984
Methodology: https://510kreport.com/methodology