FDA 510(k)

Soundly Anti Snoring Device

K-번호: K220330 · 2022-09-08

결정일2022-09-08

제품 코드LRK

자문 위원회DE

결정Substantially Equivalent

기기 요약

Soundly Anti Snoring Device is the device name listed in this FDA 510(k) record. The listed applicant is Greystone Ip, Ltd.. It received FDA 510(k) clearance on 2022-09-08 under 510(k) number K220330. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

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. The listed applicant is Greystone Ip, Ltd.. The 510(k) number is K220330.

When did Soundly Anti Snoring Device receive FDA 510(k) clearance?

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

Who is the listed applicant for Soundly Anti Snoring Device?

The FDA 510(k) record lists Greystone Ip, Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

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

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Soundly Anti Snoring Device

기기 요약

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관련 임상시험

관련 기기 (코드: LRK)

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