Class Class II

Ambu® aScope™ 5 Uretero (Standard Deflection); Ambu® aScope™ 5 Uretero (Reverse Deflection); Ambu® aView™ 2 Advance (K242108)

K242108 2024-08-16 Special
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Description

Ambu® aScope™ 5 Uretero (Standard Deflection); Ambu® aScope™ 5 Uretero (Reverse Deflection); Ambu® aView™ 2 Advance by Ambu A/S — FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242108
Clearance Date2024-08-16
Clearance TypeSpecial
Product CodeFGB
Regulation Number876.1500

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