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FDA 510(k)

THE MOSES APPLIANCE

K-Number: K093710 · 2010-05-12

ApplicantAllen J. Moses, Dds, Ltd.
Decision Date2010-05-12
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THE MOSES APPLIANCE is the device name listed in this FDA 510(k) record. The listed applicant is Allen J. Moses, Dds, Ltd.. It received FDA 510(k) clearance on 2010-05-12 under 510(k) number K093710. 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 THE MOSES APPLIANCE?

THE MOSES APPLIANCE is a medical device that received FDA 510(k) clearance on 2010-05-12. The listed applicant is Allen J. Moses, Dds, Ltd.. The 510(k) number is K093710.

When did THE MOSES APPLIANCE receive FDA 510(k) clearance?

THE MOSES APPLIANCE received FDA 510(k) clearance on 2010-05-12, under 510(k) number K093710.

Who is the listed applicant for THE MOSES APPLIANCE?

The FDA 510(k) record lists Allen J. Moses, Dds, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE MOSES APPLIANCE?

The FDA product code for THE MOSES APPLIANCE is LRK.

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Other records listing Allen J. Moses, Dds, Ltd. 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.

K160123Apinator

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.

K262104Anti Snoring Mouthpiece (L09-BB, L09-PP, L09-TB, L09-BT, L09-TP, L09-PT, L09-TT)Ram.Shaw Pte., Ltd.K261912SnØreNegatØrDnB Innovations, LLCK261366VirtusSomnomed, Inc.K261251Snorbliss® Anti-Snoring DeviceEndeavor Commerce, LLCK261134Dormiva Anti-Snoring Mouth GuardKoncept Innovators, Inc.K252942ShaeferHShaeferh, LLC

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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