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FDA 510(k)

EQ Balance

K-Number: K190735 · 2019-08-16

ApplicantUpright Science, Inc.
Decision Date2019-08-16
Product CodeLXV
DecisionSubstantially Equivalent

Device Summary

EQ Balance is the device name listed in this FDA 510(k) record. The listed applicant is Upright Science, Inc.. It received FDA 510(k) clearance on 2019-08-16 under 510(k) number K190735. The device is classified under product code LXV. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EQ Balance?

EQ Balance is a medical device that received FDA 510(k) clearance on 2019-08-16. The listed applicant is Upright Science, Inc.. The 510(k) number is K190735.

When did EQ Balance receive FDA 510(k) clearance?

EQ Balance received FDA 510(k) clearance on 2019-08-16, under 510(k) number K190735.

Who is the listed applicant for EQ Balance?

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

What is the FDA product code for EQ Balance?

The FDA product code for EQ Balance is LXV.

Related Devices (Code: LXV)

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.

K220231GyroStimUltrathera Technologies, Inc.K200529OrionInteracoustics A/SK192652TRVInteracoustics A/SK183661ClearEdge Balance SystemQuadrant BiosciencesK173669K-D BalanceKing-Devick Technologies, Inc.

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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