Class Class II

Ambu® aScope™ 5 Cysto HD (Standard Deflection); Ambu® aScope™ 5 Cysto HD (Reverse Deflection); Ambu® aView™ 2 Advance (K240848)

K240848 2024-10-10 Traditional
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Description

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

Regulatory Information

Device ClassClass Class II
510(k) NumberK240848
Clearance Date2024-10-10
Clearance TypeTraditional
Product CodeFAJ
Regulation Number876.1500

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