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FDA 510(k)

XEROS DRY MOUTH PUMP

K-Number: K110116 · 2011-04-08

ApplicantLorin Technologies Corporation
Decision Date2011-04-08
Product CodeLFD
DecisionSubstantially Equivalent

Device Summary

XEROS DRY MOUTH PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Lorin Technologies Corporation. It received FDA 510(k) clearance on 2011-04-08 under 510(k) number K110116. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XEROS DRY MOUTH PUMP?

XEROS DRY MOUTH PUMP is a medical device that received FDA 510(k) clearance on 2011-04-08. The listed applicant is Lorin Technologies Corporation. The 510(k) number is K110116.

When did XEROS DRY MOUTH PUMP receive FDA 510(k) clearance?

XEROS DRY MOUTH PUMP received FDA 510(k) clearance on 2011-04-08, under 510(k) number K110116.

Who is the listed applicant for XEROS DRY MOUTH PUMP?

The FDA 510(k) record lists Lorin Technologies Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for XEROS DRY MOUTH PUMP?

The FDA product code for XEROS DRY MOUTH PUMP 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.

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