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FDA 510(k)

Maxpower Relief

K-Number: K182120 · 2019-01-10

ApplicantOmron Healthcare, Inc.
Decision Date2019-01-10
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Maxpower Relief is the device name listed in this FDA 510(k) record. The listed applicant is Omron Healthcare, Inc.. It received FDA 510(k) clearance on 2019-01-10 under 510(k) number K182120. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Maxpower Relief?

Maxpower Relief is a medical device that received FDA 510(k) clearance on 2019-01-10. The listed applicant is Omron Healthcare, Inc.. The 510(k) number is K182120.

When did Maxpower Relief receive FDA 510(k) clearance?

Maxpower Relief received FDA 510(k) clearance on 2019-01-10, under 510(k) number K182120.

Who is the listed applicant for Maxpower Relief?

The FDA 510(k) record lists Omron Healthcare, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Maxpower Relief?

The FDA product code for Maxpower Relief is NUH.

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Related Devices (Code: NUH)

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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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