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FDA 510(k)

SNOAR(TM) OPEN AIRWAY APPLIANCE

K-Number: K880956 · 1988-05-11

ApplicantKent J. Toone, D.D.S.
Decision Date1988-05-11
Product CodeLQZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SNOAR(TM) OPEN AIRWAY APPLIANCE is the device name listed in this FDA 510(k) record. The listed applicant is Kent J. Toone, D.D.S.. It received FDA 510(k) clearance on 1988-05-11 under 510(k) number K880956. The device is classified under product code LQZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNOAR(TM) OPEN AIRWAY APPLIANCE?

SNOAR(TM) OPEN AIRWAY APPLIANCE is a medical device that received FDA 510(k) clearance on 1988-05-11. The listed applicant is Kent J. Toone, D.D.S.. The 510(k) number is K880956.

When did SNOAR(TM) OPEN AIRWAY APPLIANCE receive FDA 510(k) clearance?

SNOAR(TM) OPEN AIRWAY APPLIANCE received FDA 510(k) clearance on 1988-05-11, under 510(k) number K880956.

Who is the listed applicant for SNOAR(TM) OPEN AIRWAY APPLIANCE?

The FDA 510(k) record lists Kent J. Toone, D.D.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SNOAR(TM) OPEN AIRWAY APPLIANCE?

The FDA product code for SNOAR(TM) OPEN AIRWAY APPLIANCE is LQZ.

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Related Devices (Code: LQZ)

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.

K233754AIO BreatheAiomega, LLCK230532RADx Intraoral Appliance for Snoring and Sleep ApneaAchaemenid, LLCK203712The SlideBiotex, Inc.K191320Slow Wave DS8Slow Wave, Inc.K192581The NightBlocks ApplianceAdvanced Facialdontics, LLCK162816SML-OSA2 AppliancesSelane Products, Inc.

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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