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Chartis Precision Catheter

Page Type
Cleared 510(K)
510(k) Number
K222340
510(k) Type
Traditional
Applicant
Pulmonx Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2022
Days to Decision
120 days
Submission Type
Summary

Chartis Precision Catheter

Page Type
Cleared 510(K)
510(k) Number
K222340
510(k) Type
Traditional
Applicant
Pulmonx Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2022
Days to Decision
120 days
Submission Type
Summary