# MFD: Cannula, Intrauterine Insemination

- Device class: 2; regulation: 21 CFR 884.5250; FDA's rule: 510(k) required
- FDA decisions: 29
- Recalls: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026; MAUDE to Sep 30, 2026

## Decisions per year (last 10)
- 1992: 1
- 1993: 4
- 1994: 3
- 1995: 5
- 1996: 3
- 1997: 4
- 1998: 2
- 1999: 2
- 2001: 1
- 2002: 1

## Most-cited predicates
- K972823: Mini-Embryon Intra Uterine Insemination Catheter (1997), cited by 4
- K914150: Jansen-Anderson Insemination Set (1992), cited by 3
- K964848: Wallace Artificial Insemination Catheter - 8CM/18CM (1997), cited by 3
- K931630: Insemi-Cath (1994), cited by 2
- K910577: Edwards-Wallace Bourne Hall Catheter (1991), cited by 2
- K921518: Lifetek Iui Catheter (1994), cited by 1
- K012935: Thecurve, Item 507 (2001), cited by 1
- K954398: Insemi-Cath II (1995), cited by 1
- K972245: Tom Cat F.L., Tom Cat S.L. (1997), cited by 1
- K940176: Ackrad Iui Set for Intrauterine Insemination (1996), cited by 1

Source page: https://510kreport.com/product-code/MFD
Data by year (CSV): https://510kreport.com/product-code/MFD.csv