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FDA 510(k)

MPowRx Snoring Solution (also known as Good Morning Snore Solution)

K-Number: K193239 · 2020-01-03

ApplicantMpowrx Health and Wellness Products 2012, Inc.
Decision Date2020-01-03
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MPowRx Snoring Solution (also known as Good Morning Snore Solution) is a medical device manufactured by Mpowrx Health and Wellness Products 2012, Inc.. It received FDA 510(k) clearance on 2020-01-03 under approval number K193239. 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 MPowRx Snoring Solution (also known as Good Morning Snore Solution)?

MPowRx Snoring Solution (also known as Good Morning Snore Solution) is a medical device that received FDA 510(k) clearance on 2020-01-03. It is manufactured by Mpowrx Health and Wellness Products 2012, Inc.. The 510(k) number is K193239.

When was MPowRx Snoring Solution (also known as Good Morning Snore Solution) approved by the FDA?

MPowRx Snoring Solution (also known as Good Morning Snore Solution) received FDA 510(k) clearance on 2020-01-03, under approval number K193239.

What company makes MPowRx Snoring Solution (also known as Good Morning Snore Solution)?

MPowRx Snoring Solution (also known as Good Morning Snore Solution) is manufactured by Mpowrx Health and Wellness Products 2012, Inc..

What is the FDA product code for MPowRx Snoring Solution (also known as Good Morning Snore Solution)?

The FDA product code for MPowRx Snoring Solution (also known as Good Morning Snore Solution) is LRK.

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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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