Last synced on 23 February 2024 at 11:04 pm

Broncho Videoscope System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231521
510(k) Type
Traditional
Applicant
Scivita Medical Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/14/2023
Days to Decision
172 days
Submission Type
Summary

Broncho Videoscope System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231521
510(k) Type
Traditional
Applicant
Scivita Medical Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/14/2023
Days to Decision
172 days
Submission Type
Summary