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FDA 510(k)

SnoreRx

K-Number: K170825 · 2017-08-18

ApplicantApnea Sciences Corporation
Decision Date2017-08-18
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SnoreRx is the device name listed in this FDA 510(k) record. The listed applicant is Apnea Sciences Corporation. It received FDA 510(k) clearance on 2017-08-18 under 510(k) number K170825. 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 SnoreRx?

SnoreRx is a medical device that received FDA 510(k) clearance on 2017-08-18. The listed applicant is Apnea Sciences Corporation. The 510(k) number is K170825.

When did SnoreRx receive FDA 510(k) clearance?

SnoreRx received FDA 510(k) clearance on 2017-08-18, under 510(k) number K170825.

Who is the listed applicant for SnoreRx?

The FDA 510(k) record lists Apnea Sciences Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SnoreRx?

The FDA product code for SnoreRx is LRK.

Other records listing Apnea Sciences Corporation as applicant

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.

K153200SnoreRx

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, LLCK261366VirtusSomnomed, Inc.K261251Snorbliss® Anti-Snoring DeviceEndeavor Commerce, LLCK261134Dormiva Anti-Snoring Mouth GuardKoncept Innovators, Inc.K252942ShaeferHShaeferh, LLCK253845Anti Snoring Mouthpiece (L08-BP, L08-PT, L08-BT, L08-TP, L08-TB, L08-PB)Ram.Shaw Pte. , Ltd.

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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