# K092982: The Panpac Suction Curette

- Pathway: 510(k) (Traditional)
- Applicant: Panpac Medical Corporation
- Decided: Jul 26, 2010 after 301 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.
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’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K240434: RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6) (2024), 0 descendants of its own

## Indications for use
An endometrial suction curette, such as The Curette and Preferred Curette (available in 2.5 and 3.0 mm outer diameters), are devices used to remove tissue samples from the uterus for the purpose of biopsy and screening.

Source page: https://510kreport.com/device/K092982
Methodology: https://510kreport.com/methodology