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FDA 510(k)

MOUTHKOTE ORAL MOISTURIZER, MODEL 50930-098

K-Number: K062653 · 2006-10-27

ApplicantParnell Pharmaceuticals, Inc.
Decision Date2006-10-27
Product CodeLFD
DecisionSubstantially Equivalent

Device Summary

MOUTHKOTE ORAL MOISTURIZER, MODEL 50930-098 is the device name listed in this FDA 510(k) record. The listed applicant is Parnell Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 2006-10-27 under 510(k) number K062653. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOUTHKOTE ORAL MOISTURIZER, MODEL 50930-098?

MOUTHKOTE ORAL MOISTURIZER, MODEL 50930-098 is a medical device that received FDA 510(k) clearance on 2006-10-27. The listed applicant is Parnell Pharmaceuticals, Inc.. The 510(k) number is K062653.

When did MOUTHKOTE ORAL MOISTURIZER, MODEL 50930-098 receive FDA 510(k) clearance?

MOUTHKOTE ORAL MOISTURIZER, MODEL 50930-098 received FDA 510(k) clearance on 2006-10-27, under 510(k) number K062653.

Who is the listed applicant for MOUTHKOTE ORAL MOISTURIZER, MODEL 50930-098?

The FDA 510(k) record lists Parnell Pharmaceuticals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOUTHKOTE ORAL MOISTURIZER, MODEL 50930-098?

The FDA product code for MOUTHKOTE ORAL MOISTURIZER, MODEL 50930-098 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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