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FDA 510(k)

Zyppah Anti-Snoring Device

K-Number: K182312 · 2019-01-24

ApplicantAlways More Marketing
Decision Date2019-01-24
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Zyppah Anti-Snoring Device is the device name listed in this FDA 510(k) record. The listed applicant is Always More Marketing. It received FDA 510(k) clearance on 2019-01-24 under 510(k) number K182312. 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 Zyppah Anti-Snoring Device?

Zyppah Anti-Snoring Device is a medical device that received FDA 510(k) clearance on 2019-01-24. The listed applicant is Always More Marketing. The 510(k) number is K182312.

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

Zyppah Anti-Snoring Device received FDA 510(k) clearance on 2019-01-24, under 510(k) number K182312.

Who is the listed applicant for Zyppah Anti-Snoring Device?

The FDA 510(k) record lists Always More Marketing as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Zyppah Anti-Snoring Device?

The FDA product code for Zyppah Anti-Snoring Device 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, 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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