FDA 510(k)

Voutia™

K-Number: K173808 · 2018-07-27

Decision Date2018-07-27

Product CodeLFD

DecisionSubstantially Equivalent

Device Summary

Voutia™ is the device name listed in this FDA 510(k) record. The listed applicant is Jeffrey Ward Cash, Dds. It received FDA 510(k) clearance on 2018-07-27 under 510(k) 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. The listed applicant is Jeffrey Ward Cash, Dds. The 510(k) number is K173808.

When did Voutia™ receive FDA 510(k) clearance?

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

Who is the listed applicant for Voutia™?

The FDA 510(k) record lists Jeffrey Ward Cash, Dds as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Voutia™?

The FDA product code for Voutia™ is LFD.

Related Devices (Code: LFD)

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.

K253778Allday Moisturizing RinseElevate Oral Care K250390CloSYS® Dry Mouth Sensitive Mouth RinseRowpar Pharmaceuticals, Inc.K240508Salivea Dry Mouth Moisturizing Gel (Dry Mouth Moisturizing Gel)Laclede, Inc.K234015Caphosol® Artifical Saliva (32 doses sachet box)Eusa Pharma (Uk) Limited K231205GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral SprayGurunanda, LLC K202689Dentilube SprayOxy2plus, LLC

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.