FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇰 Denmark

Ambu® Virobac II® Exhalation Filter

K Number: K251583 · Decision Apr 30, 2026
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
201
Applicant Total
38
Review Days
342

Basic Information

Device Name
Ambu® Virobac II® Exhalation Filter
K Number
K251583
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5260
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ambu A/S
Date Received
May 23, 2025
Decision Date
April 30, 2026
Product Code
CAH
Advisory Committee
Anesthesiology
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CAH Filter, Bacterial, Breathing-Circuit

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K Number Device Name
K250269 Ambu® aScope™ 5 Cysto HD (Standard Deflection); Ambu® aScope™ 5 Cysto HD (Reverse Deflection)
K240849 Ambu® aScope™ 5 Cysto HD (Standard Deflection); Ambu® aScope™ 5 Cysto HD (Reverse Deflection); Ambu® aBox™ 2
K240848 Ambu® aScope™ 5 Cysto HD (Standard Deflection); Ambu® aScope™ 5 Cysto HD (Reverse Deflection); Ambu® aView™ 2 Advance
K242108 Ambu® aScope™ 5 Uretero (Standard Deflection); Ambu® aScope™ 5 Uretero (Reverse Deflection); Ambu® aView™ 2 Advance
K233630 Ambu® aScope™ 5 Uretero (Standard Deflection); Ambu® aScope™ 5 Uretero (Reverse Deflection); Ambu® aBox™ 2
K233886 Ambu® aScope™ Duodeno 2, Ambu® aBox™ 2
K232919 Ambu® aScope™ Gastro Large; Ambu® aBox™ 2
K233671 Ambu® aScope™ 5 Broncho 4.2/2.2; Ambu® aScope™ 5 Broncho 2.7/1.2; Ambu® aView™ 2 Advance
K232582 Ambu® aScope™ 5 Broncho 4.2/2.2 Sampler Set
K230332 Ambu® aScope™ Colon; Ambu® aBox™ 2
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