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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 the device name listed in this FDA 510(k) record. The listed applicant is Rb Health (Us), LLC. It received FDA 510(k) clearance on 2023-03-07 under 510(k) 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. The listed applicant is Rb Health (Us), LLC. The 510(k) number is K213892.

When did Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine receive FDA 510(k) clearance?

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

Who is the listed applicant for Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine?

The FDA 510(k) record lists Rb Health (Us), LLC as the applicant. This does not by itself establish the device manufacturer.

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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