510(k) K231956

Device
F&P Optiflow+ Duet Nasal Cannula
Applicant
Fisher & Paykel Healthcare, Ltd.
510(k) number
K231956
Product code
BTT
Decision
Substantially Equivalent (SESE)
Decision date
2024-02-07
Date received
2023-07-03
Regulation
868.5450
Classification name
Humidifier, Respiratory Gas, (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
Reena Daken
Address
15 Maurice Paykel Pl., E. Tamaki Auckland NZ 2013 2013

FDA Registration Numbers

Source Documents

510(k) summary PDF

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