Last synced on 19 July 2024 at 11:05 pm

Ambu® aScope™ Duodeno 2, Ambu® aBox™ 2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233886
510(k) Type
Traditional
Applicant
Ambu A/S
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
4/16/2024
Days to Decision
130 days
Submission Type
Summary

Ambu® aScope™ Duodeno 2, Ambu® aBox™ 2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233886
510(k) Type
Traditional
Applicant
Ambu A/S
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
4/16/2024
Days to Decision
130 days
Submission Type
Summary