FDA 510(k)

SNOR LOCK

K-Number: K222475 · 2022-11-10

Decision Date2022-11-10

Product CodeLRK

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

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.

Frequently Asked Questions

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.

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.

K261912SnØreNegatØrDnB Innovations, LLC K261366VirtusSomnomed, Inc.K261251Snorbliss® Anti-Snoring DeviceEndeavor Commerce, LLC K261134Dormiva Anti-Snoring Mouth GuardKoncept Innovators, Inc.K252942ShaeferHShaeferh, LLC K253845Anti Snoring Mouthpiece (L08-BP, L08-PT, L08-BT, L08-TP, L08-TB, L08-PB)Ram.Shaw Pte. , Ltd.

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.