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FDA 510(k)

AIR LIFT/XEROSTOM ARTIFICIAL SALIVA

K-Number: K120552 · 2012-06-06

ApplicantBiocosmetics Laboratories
Decision Date2012-06-06
Product CodeLFD
DecisionSubstantially Equivalent

Device Summary

AIR LIFT/XEROSTOM ARTIFICIAL SALIVA is the device name listed in this FDA 510(k) record. The listed applicant is Biocosmetics Laboratories. It received FDA 510(k) clearance on 2012-06-06 under 510(k) number K120552. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIR LIFT/XEROSTOM ARTIFICIAL SALIVA?

AIR LIFT/XEROSTOM ARTIFICIAL SALIVA is a medical device that received FDA 510(k) clearance on 2012-06-06. The listed applicant is Biocosmetics Laboratories. The 510(k) number is K120552.

When did AIR LIFT/XEROSTOM ARTIFICIAL SALIVA receive FDA 510(k) clearance?

AIR LIFT/XEROSTOM ARTIFICIAL SALIVA received FDA 510(k) clearance on 2012-06-06, under 510(k) number K120552.

Who is the listed applicant for AIR LIFT/XEROSTOM ARTIFICIAL SALIVA?

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

What is the FDA product code for AIR LIFT/XEROSTOM ARTIFICIAL SALIVA?

The FDA product code for AIR LIFT/XEROSTOM ARTIFICIAL SALIVA 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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