Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

K-D Balance

K-Number: K173669 · 2018-04-02

ApplicantKing-Devick Technologies, Inc.
Decision Date2018-04-02
Product CodeLXV
DecisionSubstantially Equivalent

Device Summary

K-D Balance is the device name listed in this FDA 510(k) record. The listed applicant is King-Devick Technologies, Inc.. It received FDA 510(k) clearance on 2018-04-02 under 510(k) number K173669. The device is classified under product code LXV. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the K-D Balance?

K-D Balance is a medical device that received FDA 510(k) clearance on 2018-04-02. The listed applicant is King-Devick Technologies, Inc.. The 510(k) number is K173669.

When did K-D Balance receive FDA 510(k) clearance?

K-D Balance received FDA 510(k) clearance on 2018-04-02, under 510(k) number K173669.

Who is the listed applicant for K-D Balance?

The FDA 510(k) record lists King-Devick Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for K-D Balance?

The FDA product code for K-D 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 BiosciencesK190735EQ BalanceUpright Science, 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.

↑