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FDA 510(k)

Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine

K-Number: K213892 · 2023-03-07

ApplicantRb Health (Us), LLC
Decision Date2023-03-07
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine is a medical device manufactured by Rb Health (Us), LLC. It received FDA 510(k) clearance on 2023-03-07 under approval number K213892. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine?

Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine is a medical device that received FDA 510(k) clearance on 2023-03-07. It is manufactured by Rb Health (Us), LLC. The 510(k) number is K213892.

When was Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine approved by the FDA?

Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine received FDA 510(k) clearance on 2023-03-07, under approval number K213892.

What company makes Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine?

Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine is manufactured by Rb Health (Us), LLC.

What is the FDA product code for Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine?

The FDA product code for Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine is NUC.

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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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