# K140761: Kahn Uterine Cannula, Jarcho Uterine Cannula, Neal Fallopian Cannula

- Pathway: 510(k) (Special)
- Applicant: Carefusion 2200, Inc.
- Decided: Apr 21, 2014 after 26 days
- Product code: HES (Insufflator, Carbon-Dioxide, Uterotubal (And Accessories))
- Device class: 2
- Regulation: 21 CFR 884.1300
- 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. The FDA summary names its predicate without a number.
- (no number) V. Mueller Preamendment Uterine Cannulas: named in the summary without a submission number

## Indications for use
The Kahn Uterine Trigger Cannula, Jarcho Self-Retaining Uterine Cannula, and Neal Fallopian Cannula are indicated to test the patency (lack of obstruction) of the fallopian tubes by pressurizing the uterus and fallopian tubes and filling them with carbon dioxide gas.

Source page: https://510kreport.com/device/K140761
Methodology: https://510kreport.com/methodology