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 a medical device manufactured by King-Devick Technologies, Inc.. It received FDA 510(k) clearance on 2018-04-02 under approval 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. It is manufactured by King-Devick Technologies, Inc.. The 510(k) number is K173669.
When was K-D Balance approved by the FDA?
K-D Balance received FDA 510(k) clearance on 2018-04-02, under approval number K173669.
What company makes K-D Balance?
K-D Balance is manufactured by King-Devick Technologies, Inc..
What is the FDA product code for K-D Balance?
The FDA product code for K-D Balance is LXV.
Related Devices (Code: LXV)
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.