CHARTIS CONSOLE— 510(k) K111764

Substantially Equivalent

Pulmonx, Inc.

FDA 510(k) clearance K111764 for CHARTIS CONSOLE, Substantially Equivalent on 2011-11-10. Applicant: Pulmonx, Inc.. Device class: 2.

Clearance details

Applicant: Pulmonx, Inc.
Product code: Code BZG
Device class: Class 2
Regulation: 21 CFR 868.1840
Advisory panel: Anesthesiology
Date received: 2011-06-23
Decision date: 2011-11-10
Decision: Substantially Equivalent
Clearance type: Special
Location: Redwood City, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.