# K172835: GRI-Alleset Veress Needle

- Pathway: 510(k) (Traditional)
- Applicant: Gri Medical and Electronic Technology Co., Ltd.
- Decided: Jun 11, 2018 after 265 days
- Product code: HIF (Insufflator, Laparoscopic)
- Device class: 2
- Regulation: 21 CFR 884.1730
- 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 K983925 (1999). 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)
- K983925: Endopath Ultra Veress Needle, Ethicon Endo-Surgery, Inc. (1999) Summary page 4.

## Indications for use
The GRI-Alleset Veress Needle is a disposable, single-use, sterile device intended to be used in minimally-invasive abdominal procedures for the establishment of pneumoperitoneum.

Source page: https://510kreport.com/device/K172835
Methodology: https://510kreport.com/methodology