510(k) K232507

Device
Aerogen®Solo Nebulizer System
Applicant
Aerogen, Ltd.
510(k) number
K232507
Product code
CAF
Decision
Substantially Equivalent (SESE)
Decision date
2024-05-10
Date received
2023-08-18
Regulation
868.5630
Classification name
Nebulizer (Direct Patient Interface)
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Thelma Marley
Address
Galway Business Park Dangan Galway IE

FDA Registration Numbers

Source Documents

510(k) summary PDF

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