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FDA 510(k)

MPOWRX SNORING SOLUTION

K-Number: K081965 · 2008-10-27

Decision Date2008-10-27
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MPOWRX SNORING SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Mpowrx Health and Wellness Products, Inc.. It received FDA 510(k) clearance on 2008-10-27 under 510(k) number K081965. 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?

MPOWRX SNORING SOLUTION is a medical device that received FDA 510(k) clearance on 2008-10-27. The listed applicant is Mpowrx Health and Wellness Products, Inc.. The 510(k) number is K081965.

When did MPOWRX SNORING SOLUTION receive FDA 510(k) clearance?

MPOWRX SNORING SOLUTION received FDA 510(k) clearance on 2008-10-27, under 510(k) number K081965.

Who is the listed applicant for MPOWRX SNORING SOLUTION?

The FDA 510(k) record lists Mpowrx Health and Wellness Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MPOWRX SNORING SOLUTION?

The FDA product code for MPOWRX SNORING SOLUTION is LRK.

Related Clinical Trials

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.

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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