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

Ambu® aScope™ 5 Broncho 4.2/2.2 Sampler Set

K Number: K232582 · Decision Sep 20, 2023
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
238
Applicant Total
38
Review Days
26

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Basic Information

Device Name
Ambu® aScope™ 5 Broncho 4.2/2.2 Sampler Set
K Number
K232582
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
874.4680
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ambu A/S
Date Received
August 25, 2023
Decision Date
September 20, 2023
Product Code
EOQ
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
EOQ Bronchoscope (Flexible Or Rigid)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EOQ), ordered by most recent decision date.

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Other Clearances by Ambu A/S

K Number Device Name
K251583 Ambu® Virobac II® Exhalation Filter
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
K230332 Ambu® aScope™ Colon; Ambu® aBox™ 2
Search all 38 clearances from Ambu A/S →