# K240434: RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6)

- Pathway: 510(k) (Traditional)
- Applicant: Li Medical Corporation, Ltd.
- Decided: Sep 25, 2024 after 224 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
Longest line of descent: 1 generation back to K092982 (2010). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K092982: The Panpac Suction Curette, Panpac Medical Corporation (2010) Summary page 6.

## Indications for use
The "RELIEEV" Suction Curette (Flexible 3.0/ Standard 3.6) is used to remove samples of materials from the uterus and from the mucosal lining of the uterus by scraping or vacuum suction. These devices obtain tissue samples for purposes of biopsy precancer screening or they can be used for menstrual extraction.

Source page: https://510kreport.com/device/K240434
Methodology: https://510kreport.com/methodology