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FDA 510(k)

OASIS DRY MOUTH RELIEF DISCS OR OASIS MOUTH MOISTURIZING DISCS

K-Number: K041563 · 2004-08-27

ApplicantGlaxosmithkline Consumer Healthcare, L.P.
Decision Date2004-08-27
Product CodeLFD
DecisionSubstantially Equivalent

Device Summary

OASIS DRY MOUTH RELIEF DISCS OR OASIS MOUTH MOISTURIZING DISCS is the device name listed in this FDA 510(k) record. The listed applicant is Glaxosmithkline Consumer Healthcare, L.P.. It received FDA 510(k) clearance on 2004-08-27 under 510(k) number K041563. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OASIS DRY MOUTH RELIEF DISCS OR OASIS MOUTH MOISTURIZING DISCS?

OASIS DRY MOUTH RELIEF DISCS OR OASIS MOUTH MOISTURIZING DISCS is a medical device that received FDA 510(k) clearance on 2004-08-27. The listed applicant is Glaxosmithkline Consumer Healthcare, L.P.. The 510(k) number is K041563.

When did OASIS DRY MOUTH RELIEF DISCS OR OASIS MOUTH MOISTURIZING DISCS receive FDA 510(k) clearance?

OASIS DRY MOUTH RELIEF DISCS OR OASIS MOUTH MOISTURIZING DISCS received FDA 510(k) clearance on 2004-08-27, under 510(k) number K041563.

Who is the listed applicant for OASIS DRY MOUTH RELIEF DISCS OR OASIS MOUTH MOISTURIZING DISCS?

The FDA 510(k) record lists Glaxosmithkline Consumer Healthcare, L.P. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OASIS DRY MOUTH RELIEF DISCS OR OASIS MOUTH MOISTURIZING DISCS?

The FDA product code for OASIS DRY MOUTH RELIEF DISCS OR OASIS MOUTH MOISTURIZING DISCS 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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