MPowRx Snoring Solution (also known as Good Morning Snore Solution)
K-Number: K193239 · 2020-01-03
Device Summary
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. The listed applicant is Mpowrx Health and Wellness Products 2012, Inc.. The 510(k) number is K193239.
When did MPowRx Snoring Solution (also known as Good Morning Snore Solution) receive FDA 510(k) clearance?
MPowRx Snoring Solution (also known as Good Morning Snore Solution) received FDA 510(k) clearance on 2020-01-03, under 510(k) number K193239.
Who is the listed applicant for MPowRx Snoring Solution (also known as Good Morning Snore Solution)?
The FDA 510(k) record lists Mpowrx Health and Wellness Products 2012, Inc. as the applicant. This does not by itself establish the device manufacturer.
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.
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.
Official Source
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