# K010056: Uterine Manipulator Injector Cannula, Sterile, Model R 57-450

- Pathway: 510(k) (Traditional)
- Applicant: A & A Medical, Inc.
- Decided: Feb 1, 2001 after 24 days
- Product code: LKF (Cannula, Manipulator/Injector, Uterine)
- Device class: 2
- Regulation: 21 CFR 884.4530
- 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. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K051160: Manipuseal (2005), 0 descendants of its own

Source page: https://510kreport.com/device/K010056
Methodology: https://510kreport.com/methodology