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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 a medical device manufactured by Upright Science, Inc.. It received FDA 510(k) clearance on 2019-08-16 under approval 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. It is manufactured by Upright Science, Inc.. The 510(k) number is K190735.

When was EQ Balance approved by the FDA?

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

What company makes EQ Balance?

EQ Balance is manufactured by Upright Science, Inc..

What is the FDA product code for EQ Balance?

The FDA product code for EQ Balance is LXV.

Related Devices (Code: LXV)

K173669K-D BalanceKing-Devick Technologies, Inc. K183661ClearEdge Balance SystemQuadrant Biosciences K200529OrionInteracoustics A/S K192652TRVInteracoustics A/S K220231GyroStimUltrathera 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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