Last synced on 30 September 2022 at 11:05 pm

Ambu aScope 4 RhinoLaryngo Intervention

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190972
510(k) Type
Traditional
Applicant
Ambu A/S
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
7/12/2019
Days to Decision
88 days
Submission Type
Summary

Ambu aScope 4 RhinoLaryngo Intervention

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190972
510(k) Type
Traditional
Applicant
Ambu A/S
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
7/12/2019
Days to Decision
88 days
Submission Type
Summary