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PENTAX Medical ONE Pulmo Single Use Video Bronchoscope System

Page Type
Cleared 510(K)
510(k) Number
K213235
510(k) Type
Traditional
Applicant
Pentax OF America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2022
Days to Decision
447 days
Submission Type
Summary

PENTAX Medical ONE Pulmo Single Use Video Bronchoscope System

Page Type
Cleared 510(K)
510(k) Number
K213235
510(k) Type
Traditional
Applicant
Pentax OF America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2022
Days to Decision
447 days
Submission Type
Summary