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FDA 510(k)

Soundly Anti Snoring Device

K-Number: K220330 · 2022-09-08

ApplicantGreystone Ip, Ltd.
Decision Date2022-09-08
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Soundly Anti Snoring Device is a medical device manufactured by Greystone Ip, Ltd.. It received FDA 510(k) clearance on 2022-09-08 under approval number K220330. 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 Soundly Anti Snoring Device?

Soundly Anti Snoring Device is a medical device that received FDA 510(k) clearance on 2022-09-08. It is manufactured by Greystone Ip, Ltd.. The 510(k) number is K220330.

When was Soundly Anti Snoring Device approved by the FDA?

Soundly Anti Snoring Device received FDA 510(k) clearance on 2022-09-08, under approval number K220330.

What company makes Soundly Anti Snoring Device?

Soundly Anti Snoring Device is manufactured by Greystone Ip, Ltd..

What is the FDA product code for Soundly Anti Snoring Device?

The FDA product code for Soundly Anti Snoring Device is LRK.

Related Clinical Trials

NCT04092660 Increasing the Use of an Anti-snoring Mouth Guard (Mandibular Advancement Appliance) to Prevent Upper Airway Collapse During Sleep in Patients With Obstructive Sleep Apnoea. RECRUITING

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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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