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FDA 510(k)

NORAD NOCTURNAL ORAL AIRWAY DILATOR APPLIANCE

K-Number: K020893 · 2002-05-28

Decision Date2002-05-28
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NORAD NOCTURNAL ORAL AIRWAY DILATOR APPLIANCE is the device name listed in this FDA 510(k) record. The listed applicant is Dennis R. Bailey, Dds. It received FDA 510(k) clearance on 2002-05-28 under 510(k) number K020893. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORAD NOCTURNAL ORAL AIRWAY DILATOR APPLIANCE?

NORAD NOCTURNAL ORAL AIRWAY DILATOR APPLIANCE is a medical device that received FDA 510(k) clearance on 2002-05-28. The listed applicant is Dennis R. Bailey, Dds. The 510(k) number is K020893.

When did NORAD NOCTURNAL ORAL AIRWAY DILATOR APPLIANCE receive FDA 510(k) clearance?

NORAD NOCTURNAL ORAL AIRWAY DILATOR APPLIANCE received FDA 510(k) clearance on 2002-05-28, under 510(k) number K020893.

Who is the listed applicant for NORAD NOCTURNAL ORAL AIRWAY DILATOR APPLIANCE?

The FDA 510(k) record lists Dennis R. Bailey, Dds as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NORAD NOCTURNAL ORAL AIRWAY DILATOR APPLIANCE?

The FDA product code for NORAD NOCTURNAL ORAL AIRWAY DILATOR APPLIANCE is LRK.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Dennis R. Bailey, Dds as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: LRK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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

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