# K020628: Curelle, Preferred Curelle, Cuteq 2.5

- Pathway: 510(k) (Traditional)
- Applicant: Bioteque America, Inc.
- Decided: May 24, 2002 after 87 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.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Indications for use
The suction curettes (Preferred Curette, Curelle or Cuteq 2.5) are used to remove products of conception and obtain samples from the endometrial cavity by vacuum suction.

Source page: https://510kreport.com/device/K020628
Methodology: https://510kreport.com/methodology