# K940681: Clearview Uterine Manipulator

- Pathway: 510(k) (Traditional)
- Applicant: Clinical Innovations, Inc.
- Decided: Jul 26, 1994 after 166 days
- Product code: LKF (Cannula, Manipulator/Injector, Uterine)
- Device class: 2
- Regulation: 21 CFR 884.4530
- Recalls of this device: 2 (0 Class I)
- 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; 1 cites 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
- K131781: Clearview Total (2014), 1 descendant of its own
- K172846: Uterine Manipulator (2018), 0 descendants of its own

## Recalls of this device
- May 12, 2008 · Not classified · Z-1818-2008: Inadequate package seal could compromise sterility.
- May 12, 2008 · Not classified · Z-1817-2008: Inadequate package seal could compromise sterility.

Source page: https://510kreport.com/device/K940681
Methodology: https://510kreport.com/methodology