FDA 510(k)

SNOR LOCK

Número K: K222475 · 2022-11-10

Data da decisão2022-11-10

Código do produtoLRK

Comité consultivoDE

DecisãoSubstantially Equivalent

Resumo do dispositivo

SNOR LOCK is the device name listed in this FDA 510(k) record. The listed applicant is Solbaro Co., Ltd.. It received FDA 510(k) clearance on 2022-11-10 under 510(k) number K222475. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the SNOR LOCK?

SNOR LOCK is a medical device that received FDA 510(k) clearance on 2022-11-10. The listed applicant is Solbaro Co., Ltd.. The 510(k) number is K222475.

When did SNOR LOCK receive FDA 510(k) clearance?

SNOR LOCK received FDA 510(k) clearance on 2022-11-10, under 510(k) number K222475.

Who is the listed applicant for SNOR LOCK?

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

What is the FDA product code for SNOR LOCK?

The FDA product code for SNOR LOCK is LRK.

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Fonte oficial

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