510(k) K253096

Device
Chartis Precision Catheter
Applicant
Pulmonx Corporation
510(k) number
K253096
Product code
CBI
Decision
Substantially Equivalent (SESE)
Decision date
2026-02-13
Date received
2025-09-23
Regulation
868.5740
Classification name
Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Leah Andre
Address
700 Chesapeake Dr. Redwood City CA US 94063 94063

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code CBI#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
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K222340Chartis Precision CatheterPulmonx Corporation2022-12-01
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K181886VivaSight-DL SystemEtview , Ltd.2018-11-14
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K1605425.0 Fr Arndt Endobronchial Blocker SetCook Incorporated2016-08-02
K152251Endobronchial TubeHenan Tuoren Medical Device Co., Ltd.2016-06-10
K141888RUSCH ENDOBRONCHIAL TUBESTeleflexmedical, Inc.2015-04-15
K123853VIVASIGHT-DL SYSTEMEtview , Ltd.2013-04-15
K121462EZ-BLOCKEREz-Blocker B.V.2012-09-28
K120334VIVA EBEtview , Ltd.2012-06-08