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

Page Type
Cleared 510(K)
510(k) Number
K233886
510(k) Type
Traditional
Applicant
Ambua/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)
510(k) Number
K233886
510(k) Type
Traditional
Applicant
Ambua/S
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
4/16/2024
Days to Decision
130 days
Submission Type
Summary