FDA 510(k)

Caphosol Artifical Saliva Tablets

K-Number: K162167 · 2017-03-31

Decision Date2017-03-31

Product CodeLFD

DecisionSubstantially Equivalent

Device Summary

Caphosol Artifical Saliva Tablets is a medical device manufactured by Eusa Pharma (Uk) Limited. It received FDA 510(k) clearance on 2017-03-31 under approval number K162167. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Caphosol Artifical Saliva Tablets?

Caphosol Artifical Saliva Tablets is a medical device that received FDA 510(k) clearance on 2017-03-31. It is manufactured by Eusa Pharma (Uk) Limited. The 510(k) number is K162167.

When was Caphosol Artifical Saliva Tablets approved by the FDA?

Caphosol Artifical Saliva Tablets received FDA 510(k) clearance on 2017-03-31, under approval number K162167.

What company makes Caphosol Artifical Saliva Tablets?

Caphosol Artifical Saliva Tablets is manufactured by Eusa Pharma (Uk) Limited.

What is the FDA product code for Caphosol Artifical Saliva Tablets?

The FDA product code for Caphosol Artifical Saliva Tablets is LFD.

Other Devices by Eusa Pharma (Uk) Limited

K234015Caphosol® Artifical Saliva (32 doses sachet box)

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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.