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FDA 510(k)

AIRLIFE DEMAND NASAL CANNULA

K-Number: K023673 · 2003-05-02

ApplicantAllegiance Healthcare Corp.
Decision Date2003-05-02
Product CodeNFB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AIRLIFE DEMAND NASAL CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Allegiance Healthcare Corp.. It received FDA 510(k) clearance on 2003-05-02 under 510(k) number K023673. The device is classified under product code NFB. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIRLIFE DEMAND NASAL CANNULA?

AIRLIFE DEMAND NASAL CANNULA is a medical device that received FDA 510(k) clearance on 2003-05-02. The listed applicant is Allegiance Healthcare Corp.. The 510(k) number is K023673.

When did AIRLIFE DEMAND NASAL CANNULA receive FDA 510(k) clearance?

AIRLIFE DEMAND NASAL CANNULA received FDA 510(k) clearance on 2003-05-02, under 510(k) number K023673.

Who is the listed applicant for AIRLIFE DEMAND NASAL CANNULA?

The FDA 510(k) record lists Allegiance Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIRLIFE DEMAND NASAL CANNULA?

The FDA product code for AIRLIFE DEMAND NASAL CANNULA is NFB.

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Other records listing Allegiance Healthcare Corp. as applicant

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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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