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FDA 510(k)

F&P Optiflow+ Duet Nasal Cannula

K-Number: K231956 · 2024-02-07

ApplicantFisher & Paykel Healthcare, Ltd.
Decision Date2024-02-07
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

F&P Optiflow+ Duet Nasal Cannula is a medical device manufactured by Fisher & Paykel Healthcare, Ltd.. It received FDA 510(k) clearance on 2024-02-07 under approval number K231956. The device is classified under product code BTT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the F&P Optiflow+ Duet Nasal Cannula?

F&P Optiflow+ Duet Nasal Cannula is a medical device that received FDA 510(k) clearance on 2024-02-07. It is manufactured by Fisher & Paykel Healthcare, Ltd.. The 510(k) number is K231956.

When was F&P Optiflow+ Duet Nasal Cannula approved by the FDA?

F&P Optiflow+ Duet Nasal Cannula received FDA 510(k) clearance on 2024-02-07, under approval number K231956.

What company makes F&P Optiflow+ Duet Nasal Cannula?

F&P Optiflow+ Duet Nasal Cannula is manufactured by Fisher & Paykel Healthcare, Ltd..

What is the FDA product code for F&P Optiflow+ Duet Nasal Cannula?

The FDA product code for F&P Optiflow+ Duet Nasal Cannula is BTT.

Related Clinical Trials

NCT07613762 High-Flow Nasal Cannula on Exercise Tolerance in Heart Failure Patients Undergoing Cardiac Rehabilitation. NOT_YET_RECRUITING NCT06671015 A Trial Comparing High-Flow Nasal Cannula Versus Noninvasive Ventilation on Reintubation and Post-Extubation Respiratory Failure in High-Risk Patients With Systolic Heart Failure RECRUITING NCT07611903 HFNC Versus Microstream Advance Nasal Cannula for Oxygenation During ERCP NOT_YET_RECRUITING NCT07234188 POM vs HFNC for Hypoxemia Prevention in Children COMPLETED NCT07600333 CPAP vs High-Flow Nasal Cannula for Treating Sleep Apnea in Children NOT_YET_RECRUITING NCT07564050 Physiological Effects of Different Preoxygenation Strategies RECRUITING

Other Devices by Fisher & Paykel Healthcare, Ltd.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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