# Pulmonx Corporation

- Location (FDA's records): Redwood City, CA
- FDA decisions: 10 (1998–2026): 9 510(k) clearances and 1 original PMA approval
- Names in FDA's records: Pulmonx Corporation (5); Pulmonx, Inc. (4); Pulmonx (1)
- Product codes: CBI (4), BZG (3), BTR (1), JAK (1), NJK (1)
- Predicates its devices cite: 7 (5 its own); citations of its devices by later devices: 6 (5 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Thirona BV: 1 (https://510kreport.com/company/thirona)
- Cook, Inc.: 1 (https://510kreport.com/company/cook)

## Firms that cite its devices most
- Etview, Ltd.: 1 (https://510kreport.com/company/etview)

## Its most-cited devices
- K083199: Chartis Console (2009), cited by 1
- K222340: Chartis Precision Catheter (2022), cited by 1
- K973191: The Visualized Endotracheal Tube System or Vett System (1998), cited by 1
- K111764: Chartis Console (2011), cited by 1
- K083883: Chartis Catheter (2009), cited by 1
- K111522: Chartis Catheter Model CHR-CA-12.0 (2011), cited by 1

## Recent decisions
- K253096: Chartis Precision Catheter (Feb 13, 2026)
- K222340: Chartis Precision Catheter (Dec 1, 2022)
- K212494: Lung Image Analysis (Sep 2, 2021)
- K180011: Pulmonx Chartis Tablet Console (Jul 13, 2018)
- P180002: Zephyr Endobronchial Valve System (Jun 29, 2018)
- K111764: Chartis Console (Nov 10, 2011)
- K111522: Chartis Catheter Model CHR-CA-12.0 (Sep 29, 2011)
- K083199: Chartis Console (Jun 25, 2009)

Source page: https://510kreport.com/company/pulmonx