# K931630: Insemi-Cath

- Pathway: 510(k) (Traditional)
- Applicant: Cook Ob/Gyn
- Decided: Apr 19, 1994 after 382 days
- Product code: MFD (Cannula, Intrauterine Insemination)
- Device class: 2
- Regulation: 21 CFR 884.5250
- 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. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K984306: `the Inseminator' (Proposed) (1999), 0 descendants of its own
- K980061: Embryon Intrauterine Insemination Catheter, Emryon Soft Intrauterine Insemination Catheter, Stylet for Embryon Intrauter (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K931630
Methodology: https://510kreport.com/methodology