510(k) K233671

Device
Ambu® aScope? 5 Broncho 4.2/2.2; Ambu® aScope? 5 Broncho 2.7/1.2; Ambu® aView? 2 Advance
Applicant
Ambu A/S
510(k) number
K233671
Product code
EOQ
Decision
Substantially Equivalent (SESE)
Decision date
2024-01-04
Date received
2023-11-15
Regulation
874.4680
Classification name
Bronchoscope (Flexible Or Rigid)
Medical specialty
Ear, Nose, Throat
Review panel
Ear, Nose, Throat
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Lasse Sohrt-Petersen
Address
Baltorpbakken 13 Ballerup DK 2750 2750

FDA Registration Numbers

Source Documents

510(k) summary PDF

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