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FDA 510(k)

GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray

K-Number: K231205 · 2023-08-22

ApplicantGurunanda, LLC
Decision Date2023-08-22
Product CodeLFD
DecisionSubstantially Equivalent

Device Summary

GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray is a medical device manufactured by Gurunanda, LLC. It received FDA 510(k) clearance on 2023-08-22 under approval number K231205. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray?

GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray is a medical device that received FDA 510(k) clearance on 2023-08-22. It is manufactured by Gurunanda, LLC. The 510(k) number is K231205.

When was GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray approved by the FDA?

GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray received FDA 510(k) clearance on 2023-08-22, under approval number K231205.

What company makes GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray?

GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray is manufactured by Gurunanda, LLC.

What is the FDA product code for GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray?

The FDA product code for GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray is LFD.

Related Clinical Trials

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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