FDA 510(k)

Voutia

K-Number: K173808 · 2018-07-27

Decision Date2018-07-27

Product CodeLFD

DecisionSubstantially Equivalent

Device Summary

Voutia is a medical device manufactured by Jeffrey Ward Cash, Dds. It received FDA 510(k) clearance on 2018-07-27 under approval number K173808. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Voutia?

Voutia is a medical device that received FDA 510(k) clearance on 2018-07-27. It is manufactured by Jeffrey Ward Cash, Dds. The 510(k) number is K173808.

When was Voutia approved by the FDA?

Voutia received FDA 510(k) clearance on 2018-07-27, under approval number K173808.

What company makes Voutia?

Voutia is manufactured by Jeffrey Ward Cash, Dds.

What is the FDA product code for Voutia?

The FDA product code for Voutia is LFD.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.