# K132203: Pneuview XE Veryclear Gas Evacuation Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Lexion Medical, LLC
- Decided: Sep 20, 2013 after 66 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: 7 generations back to K964171 (1997). 34 ancestors in all.
No later device cites it as a predicate yet.
0 of 35 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K103692: Sugiquest Airsealoptical Trocar & Cannula System with Integrated Insufflator Dpis 2000, Surgiquest, Inc. (2011) Summary page 1.
- K120640: Insuflow Synergy Port, Lexion Medical, LLC (2012) Summary page 1.
- (no number) PneuVIEW®XE Smoke Evacuation System: named in the summary without a submission number

## Indications for use
PneuVIEW® XE VeryClear™ Gas Evacuation Cannula has applications in thoracic, abdominal and gynecologic minimally invasive endoscopic surgical procedures to establish a path of entry for endoscopic instruments and to evacuate smoke and plume generated during minimally invasive surgery from the surgical cavity to aid visualization.

Source page: https://510kreport.com/device/K132203
Methodology: https://510kreport.com/methodology