# K012935: Thecurve, Item 507

- Pathway: 510(k) (Traditional)
- Applicant: Select Medical Systems, Inc.
- Decided: Oct 11, 2001 after 41 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.
1 later device descends from it; 1 cites it directly.
0 of 2 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 its predicate without a number.
- (no number) Select IUI®: named in the summary without a submission number

## Most influential descendants
- K143669: MedGyn Straight IUI Catheter, MedGyn Mini IUI Catheter, MedGyn curved, mini IUI Catheter (2015), 0 descendants of its own

## Indications for use
Intrauterine artificial insemination

Source page: https://510kreport.com/device/K012935
Methodology: https://510kreport.com/methodology