# K881456: Pipelle DE Cornier Endometrial Suction Curette

- Pathway: 510(k) (Traditional)
- Applicant: Laboratoire Ccd C/O Washington Regulatory Services
- Decided: Oct 14, 1988 after 191 days
- Product code: HHK (Curette, Suction, Endometrial (And Accessories))
- Device class: 2
- Regulation: 21 CFR 884.1175
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
6 later devices descend from it; 2 cite it directly.
0 of 7 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
- K082066: Tao Brush I.U.M.C. Endometrial Sampler (2008), 4 descendants of its own
- K170603: Tao Brush I.U.M.C. Endometrial Sampler (2017), 1 descendant of its own
- K240595: Utepreva Endometrial Sampler (UP01) (2024), 0 descendants of its own
- K133144: Sonosure Sonohysterography & Endometrial Sampling Device (2014), 0 descendants of its own
- K112763: Matrixbrush Endometrial Sampler (2012), 0 descendants of its own

Source page: https://510kreport.com/device/K881456
Methodology: https://510kreport.com/methodology