Last synced on 30 September 2022 at 11:05 pm

Broncoflex Agile, Broncoflex Vortex, Screeni

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212886
510(k) Type
Traditional
Applicant
Axess Vision Technology
Country
France
FDA Decision
Substantially Equivalent
Decision Date
2/16/2022
Days to Decision
159 days
Submission Type
Summary

Broncoflex Agile, Broncoflex Vortex, Screeni

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212886
510(k) Type
Traditional
Applicant
Axess Vision Technology
Country
France
FDA Decision
Substantially Equivalent
Decision Date
2/16/2022
Days to Decision
159 days
Submission Type
Summary